What the tender required and what the award supports
Source material and existing AI analysis appear first. Supplier conclusions remain qualified by the evidence Tenders-SA holds.
Summary
This tender invites bids for the supply, delivery, installation, demonstration, and commissioning of blood gas analysers under a 3-year consumable placement deal for western cape government health and wellness facilities. The contract covers 31 facilities, with the contractor retaining equipment ownership while supplying consumables monthly.
Document read. The full tender notice and its supporting documents are read end-to-end. Key sections, requirements, dates, and contact details are identified and pulled into a working summary you can act on.
Compliance review. The working summary is checked against South African procurement standards — PFMA, PPPFA, B-BBEE, CIDB, local content, and preferential procurement — so nothing critical is missed before you start your bid response.
0 of 1 source documents fully reviewed. Unstated details are identified only after complete source review.
technical scope
4 sourced criteria
financial capacity
1 sourced criteria
pricing
2 sourced criteria
compliance returnables
Source analysis requires completion or review
evaluation
3 sourced criteria
experience
2 sourced criteria
personnel
1 sourced criteria
equipment capacity
1 sourced criteria
delivery contract
Source analysis requires completion or review
equity registrations
4 sourced criteria
What the buyer was looking for
1Mandatory requirement
Bidders must be registered on the Central Supplier Database (CSD) and tax-compliant by bid closing (10 July 2026, 11:00).
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
The linked award records MEDHOLD MEDICAL as appointed for this tender.
Qualified inference
Inference only
An award confirms appointment. It does not prove why a supplier was selected, that every qualification remains current, or that delivery was completed successfully.
Bid-ready summary. The submission guidelines, evaluation criteria, technical, financial, and compliance sections are refined into professional, easy-to-scan prose. This is the final version you can rely on when preparing your bid or briefing your team.
We refine every tender document through these stages so you can brief your team and prepare your bid with confidence. Anything marked as "in progress" will be upgraded automatically — no action required from you.
Scope: Supply, delivery, installation, demonstration, and commissioning of blood gas analysers under a 3-year consumable placement deal for 31 Western Cape health facilities. Equipment is placed at no cost to the department; only consumables (cartridges, syringes) are procured monthly. Contractor retains ownership of equipment for the 3-year period. Facilities can adjust consumable orders monthly without penalty. Department may add facilities if need arises. Total cost of ownership must be clearly described, including cost per test.
Closing date: 10 July 2026 at 11:00. Bid validity period: 120 days from closing date (expires 07 November 2026). Query deadline: End of business, 26 June 2026. Department response to queries: End of business, 30 June 2026. Evaluation trial period: 4 weeks (units must be available within 2 weeks of official request).
Submit bids by 11:00 on 10 July 2026. Hard copy must be deposited in a sealed envelope, marked with bidder name, bid number, and closing date, into the bid box marked 'Department of Health' at Supply Chain Management Offices (M9 building), Karl Bremer Hospital, c/o Mike Pienaar Boulevard & Frans Conradie Avenue, Bellville. Office hours: Monday to Friday, 07:30–16:00 (excluding public holidays). A soft copy on USB must also be submitted. Hard copy supersedes electronic copy if discrepancies exist. Late submissions, fax, email, or telegram submissions will not be accepted. Ensure all pages are included, signed in original black ink, and no alterations are made to the bid documents. Bidders must confirm bid document download via email to [email protected] and [email protected] with company name, contact person, phone number, and email address. Bids must be submitted on official forms provided; do not re-type or redraft. Only original, signed documents will be considered. Photocopies may be prepared for bidder records. No pages may be omitted or duplicated. Failure to submit requested information may result in disqualification. Bids submitted by security personnel or without proper authority will not be accepted. Queries about bid box location must be directed to the listed officials, not security personnel.
Evaluation occurs in three phases: Phase 1: Compliance with specifications, pricing, and all mandatory requirements. Phase 2: 4-week trial with 3 machines at Mitchells Plain and Victoria Hospitals; evaluator report compiled. Phase 3: Final recommendation considering all inputs, followed by application of the 80:20 Preferential Procurement Points System (80 points for price, 20 points for B-BBEE). Only the B-BBEE status declared on the WCBD 6.1 form is considered for evaluation. Cost per test (including all relevant costs such as maintenance, consumables, and syringes) and real-world functionality experiences are key factors. Non-compliant bidders will be notified after the bid process concludes. The Department reserves the right to award the bid in part or in whole based on compliance, clinical acceptability, price, and preference points.
Supply, deliver, install, demonstrate, and commission blood gas analysers under a 3-year consumable placement deal for 31 Western Cape health facilities. Equipment remains the contractor’s property; only consumables (cartridges, syringes) are procured monthly. Contractor retains ownership of equipment for the 3-year period. Facilities can adjust consumable orders monthly without penalty. Department may add facilities if need arises. Total cost of ownership must be clearly described, including cost per test. Key requirements for analysers: Latest technology for adult/paediatric care, test cycle ≤120 seconds, sample volume 60–70µl (preference for <50µl), 8" touchscreen, daily auto QC/calibration, UPS for 1-hour backup, printer, memory for ≥3500 results and ≥2000 patients, user PIN access, blood clot prevention system, and waste containment. Must include pre-heparinised syringes/capillaries in monthly cost. Cartridges must offer all parameters (excluding cCrea optionally) with shelf life ≥3 months (12 months for syringes). 24/7 support with 24-hour response time; replacement units provided if repairs exceed 24 hours. Delivery of consumables within 48 hours of request. OEM support letter required. Evaluation includes 4-week trial at Mitchells Plain and Victoria Hospitals. Bidders must provide proof of being an accredited supplier of the offered devices by the OEM, with OEM commitment to provide expertise, training, and support. Technical staff must be factory-trained; provide names, locations of repair centres in Western Cape, and competency certificates. Number of technicians employed in Western Cape and repair facility addresses required. Training for hospital staff (users and clinical engineering) must be provided at no extra cost. Preventative maintenance and calibration procedures must be provided. Workshop/Service Manuals are mandatory. Random quality compliance testing of samples from institutions throughout contract. Department reserves right to inspect bidder’s repair facilities and validate technical staff competency.
Bidders must provide: Proof of being an accredited supplier of offered devices by the OEM, with OEM commitment to provide expertise, training, and support. List of sites with similar installed machines for reference. Technical staff must be factory-trained; provide names, locations of repair centres in Western Cape, and competency certificates. Number of technicians employed in Western Cape and repair facility addresses required. Department reserves right to inspect facilities. Training for hospital staff (users and clinical engineering) must be provided at no extra cost, covering equipment use, resetting, cleaning, flushing, and calibration.
Mandatory: ISO 13485 certification for each manufacturer of offered products. Random quality compliance testing of samples from institutions throughout contract. Bidders must provide approval/validation report from an accredited SANAS laboratory for the offered unit. Department may request clinical evidence. All offered units must be currently marketed in South Africa with verifiable references. Department reserves the right to inspect bidder’s repair facilities and validate technical staff competency. Preventative maintenance and calibration procedures must be provided. Workshop/Service Manuals are mandatory. Packaging must include manufacturer/supplier name, bidder item name, item code, date of manufacture, product expiry date, and batch/lot number. All items must be delivered in a carton/box.
Submit pricing in ZAR, VAT-inclusive, for Year 1, Year 2, and Year 3. Cartridge cost must include all costs (maintenance, consumables, syringes). Pricing options: Firm prices (fixed for contract duration) or non-firm prices (ROE-linked or proven adjustments). For ROE-linked: ROE determined 10 days before closing (30 June 2026); max 85% imported content; claims within 60 days of delivery. Non-firm prices: No adjustments in first 3 months; quarterly thereafter. Provide cost per test, cartridge sizes, individual consumable prices, and monthly cost breakdown. Include pricing for optional accessories. Delivery costs must be included in bid price. Pricing schedule must list cost of each cartridge size and individual consumables separately, with corresponding pricing for Year 1, Year 2, and Year 3.
Pricing must be in ZAR, VAT-inclusive, and cover all costs (delivery, maintenance, consumables, syringes). Submit pricing for Year 1, Year 2, and Year 3. Options: Firm prices (fixed for contract duration) or non-firm prices (subject to ROE variations or proven adjustments). For ROE-linked prices: ROE determined 10 days before closing (30 June 2026), max 85% imported content claimable, claims within 60 days of delivery. Non-firm prices: No adjustments in first 3 months; quarterly thereafter. Include cost per test, cartridge sizes, and individual consumable pricing. Offers valid for 120 days from closing. Payment within 30 days of valid invoice via EFT. Provide banking details for LOGIS/BAS/SYSPRO registration if not already on file. Include pricing for optional accessories. Delivery costs must be included in bid price. Pricing schedule must list cost of each cartridge size and individual consumables separately, with corresponding pricing for Year 1, Year 2, and Year 3.
Mandatory: CSD registration (www.csd.gov.za) at bid closing; tax compliance must be verifiable via CSD (7-day grace period if non-compliant). Submit valid SAHPRA licence as manufacturer, distributor, or wholesaler of medical devices/IVDs (no proof of application accepted). ISO 13485 certification for each manufacturer whose products are bid. OHS Act Section 37(2) Agreement (mandatory for all procurements with on-site work or health & safety risks). B-BBEE status must be declared via WCBD 6.1 form (only this applies; not CSD status). Complete WCBD 4 (Declaration of Interests, Bidders Past SCM Practices, and Independent Bid Determination). All mandatory documents on CSD/Western Cape Supplier Evidence Bank accepted. Foreign suppliers: Provide proof of SA representation if applicable. No bids from state employees or entities with state-employed directors/members. Proof of authority to sign bids required. Tax Compliance Status (TCS) PIN or printed TCS certificate must be submitted. For consortia/joint ventures/sub-contractors, each party must submit separate TCS certificate and CSD number. Bidders must ensure compliance with their tax obligations. Contract governed by General Conditions of Contract (GCC) and Special Conditions of Contract (SCC), with SCC prevailing in conflicts.
Contract governed by General Conditions of Contract (GCC) and Special Conditions of Contract (SCC), with SCC prevailing in conflicts. 80:20 Preferential Procurement Points System applies. Offers valid for 120 days from closing. Department reserves rights to: withdraw/amend bid, terminate participation for non-compliance, reject any/all bids, or negotiate prices/service delivery. Contract may be terminated for insolvency, fraud, poor performance (after 3 warnings), or breach of specifications. Penalties include deductions for turnaround time non-adherence or specification breaches. Warranty: 12 months for defects; contractor must repair/replace within specified period. Subcontracting requires prior written approval; contractor remains liable for subcontractor compliance. Transfer, cession, or use of subcontractors requires prior written approval from the Department. Prices must include all costs and applicable taxes (VAT-inclusive). No price adjustments in first 3 months for non-firm prices; quarterly adjustments thereafter. Department reserves the right to award per institution based on bidder capability.
Evaluation is based on three phases: Phase 1: Compliance with specifications, pricing, and mandatory requirements. Phase 2: 4-week trial with 3 machines at Mitchells Plain and Victoria Hospitals; evaluator report compiled. Phase 3: Final recommendation considering all inputs, followed by application of the 80:20 Preferential Procurement Points System (80 points for price, 20 points for B-BBEE). Only the B-BBEE status declared on the WCBD 6.1 form is considered. Cost per test (including all relevant costs) and real-world functionality experiences are key factors. Non-compliant bidders will be notified after the bid process concludes.
The successful bid likely addressed this expectation, but the submitted evidence and evaluation reason are unavailable.
The linked award confirms appointment only, not the submitted qualification or reason for selection.
2Inferred operational need
Submit a valid SAHPRA licence (manufacturer/distributor/wholesaler of medical devices) and ISO 13485 certification for each manufacturer.
Why it matters: This is a qualified operational interpretation of the stored scope, not a stated mandatory or scored criterion.
Inferred from stored analysis; verify against the source document. No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
The linked award records MEDHOLD MEDICAL as appointed for this tender.
Qualified inference
Inference only
The successful bid likely addressed this expectation, but the submitted evidence and evaluation reason are unavailable.
The linked award confirms appointment only, not the submitted qualification or reason for selection.
3Inferred operational need
Deliver consumables within 48 hours of request; 24/7 support with 24-hour response time and replacement units if repairs exceed 24 hours.
Why it matters: This is a qualified operational interpretation of the stored scope, not a stated mandatory or scored criterion.
Inferred from stored analysis; verify against the source document. No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
4Inferred operational need
Submit hard copy (sealed envelope) and USB soft copy to the bid box at Karl Bremer Hospital, Bellville, by the deadline.
Why it matters: This is a qualified operational interpretation of the stored scope, not a stated mandatory or scored criterion.
Inferred from stored analysis; verify against the source document. No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
5Mandatory requirement
Pricing must be in ZAR, VAT-inclusive, and cover all costs (delivery, maintenance, consumables, syringes). Submit pricing for Year 1, Year 2, and Year 3. Options: Firm prices (fixed for contract duration) or non-firm prices (subject to ROE variations or proven adjustments). For ROE-linked prices: ROE determined 10 days before closing (30 June 2026), max 85% imported content claimable, claims within 60 days of delivery. Non-firm prices: No adjustments in first 3 months; quarterly thereafter. Include cost per test, cartridge sizes, and individual consumable pricing. Offers valid for 120 days from closing. Payment within 30 days of valid invoice via EFT. Provide banking details for LOGIS/BAS/SYSPRO registration if not already on file. Include pricing for optional accessories. Delivery costs must be included in bid price. Pricing schedule must list cost of each cartridge size and individual consumables separately, with corresponding pricing for Year 1, Year 2, and Year 3.
Threshold: 10 days
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
6Mandatory requirement
Pricing must be in ZAR (VAT-inclusive), covering delivery, maintenance, consumables, and syringes, with firm or non-firm options for Years 1–3.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
7Mandatory requirement
Submit pricing in ZAR, VAT-inclusive, for Year 1, Year 2, and Year 3. Cartridge cost must include all costs (maintenance, consumables, syringes). Pricing options: Firm prices (fixed for contract duration) or non-firm prices (ROE-linked or proven adjustments). For ROE-linked: ROE determined 10 days before closing (30 June 2026); max 85% imported content; claims within 60 days of delivery. Non-firm prices: No adjustments in first 3 months; quarterly thereafter. Provide cost per test, cartridge sizes, individual consumable prices, and monthly cost breakdown. Include pricing for optional accessories. Delivery costs must be included in bid price. Pricing schedule must list cost of each cartridge size and individual consumables separately, with corresponding pricing for Year 1, Year 2, and Year 3.
Threshold: 10 days
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
8Inferred operational need
Provide a 4-week trial with 3 machines at Mitchells Plain and Victoria Hospitals; evaluation includes cost per test and real-world functionality.
Why it matters: This is a qualified operational interpretation of the stored scope, not a stated mandatory or scored criterion.
Inferred from stored analysis; verify against the source document. No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
9Mandatory requirement
Contract governed by General Conditions of Contract (GCC) and Special Conditions of Contract (SCC), with SCC prevailing in conflicts. 80:20 Preferential Procurement Points System applies. Offers valid for 120 days from closing. Department reserves rights to: withdraw/amend bid, terminate participation for non-compliance, reject any/all bids, or negotiate prices/service delivery. Contract may be terminated for insolvency, fraud, poor performance (after 3 warnings), or breach of specifications. Penalties include deductions for turnaround time non-adherence or specification breaches. Warranty: 12 months for defects; contractor must repair/replace within specified period. Subcontracting requires prior written approval; contractor remains liable for subcontractor compliance. Transfer, cession, or use of subcontractors requires prior written approval from the Department. Prices must include all costs and applicable taxes (VAT-inclusive). No price adjustments in first 3 months for non-firm prices; quarterly adjustments thereafter. Department reserves the right to award per institution based on bidder capability.
Threshold: 120 days
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
10Mandatory requirement
Supply, deliver, install, demonstrate, and commission blood gas analysers under a 3-year consumable placement deal for 31 Western Cape health facilities. Equipment remains the contractor’s property; only consumables (cartridges, syringes) are procured monthly. Contractor retains ownership of equipment for the 3-year period. Facilities can adjust consumable orders monthly without penalty. Department may add facilities if need arises. Total cost of ownership must be clearly described, including cost per test. Key requirements for analysers: Latest technology for adult/paediatric care, test cycle ≤120 seconds, sample volume 60–70µl (preference for <50µl), 8" touchscreen, daily auto QC/calibration, UPS for 1-hour backup, printer, memory for ≥3500 results and ≥2000 patients, user PIN access, blood clot prevention system, and waste containment. Must include pre-heparinised syringes/capillaries in monthly cost. Cartridges must offer all parameters (excluding cCrea optionally) with shelf life ≥3 months (12 months for syringes). 24/7 support with 24-hour response time; replacement units provided if repairs exceed 24 hours. Delivery of consumables within 48 hours of request. OEM support letter required. Evaluation includes 4-week trial at Mitchells Plain and Victoria Hospitals. Bidders must provide proof of being an accredited supplier of the offered devices by the OEM, with OEM commitment to provide expertise, training, and support. Technical staff must be factory-trained; provide names, locations of repair centres in Western Cape, and competency certificates. Number of technicians employed in Western Cape and repair facility addresses required. Training for hospital staff (users and clinical engineering) must be provided at no extra cost. Preventative maintenance and calibration procedures must be provided. Workshop/Service Manuals are mandatory. Random quality compliance testing of samples from institutions throughout contract. Department reserves right to inspect bidder’s repair facilities and validate technical staff competency.
Threshold: 3 months
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
11Mandatory requirement
Mandatory: ISO 13485 certification for each manufacturer of offered products. Random quality compliance testing of samples from institutions throughout contract. Bidders must provide approval/validation report from an accredited SANAS laboratory for the offered unit. Department may request clinical evidence. All offered units must be currently marketed in South Africa with verifiable references. Department reserves the right to inspect bidder’s repair facilities and validate technical staff competency. Preventative maintenance and calibration procedures must be provided. Workshop/Service Manuals are mandatory. Packaging must include manufacturer/supplier name, bidder item name, item code, date of manufacture, product expiry date, and batch/lot number. All items must be delivered in a carton/box.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
12Mandatory requirement
Bidders must provide: Proof of being an accredited supplier of offered devices by the OEM, with OEM commitment to provide expertise, training, and support. List of sites with similar installed machines for reference. Technical staff must be factory-trained; provide names, locations of repair centres in Western Cape, and competency certificates. Number of technicians employed in Western Cape and repair facility addresses required. Department reserves right to inspect facilities. Training for hospital staff (users and clinical engineering) must be provided at no extra cost, covering equipment use, resetting, cleaning, flushing, and calibration.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
13Mandatory requirement
Submit bids by 11:00 on 10 July 2026. Hard copy must be deposited in a sealed envelope, marked with bidder name, bid number, and closing date, into the bid box marked 'Department of Health' at Supply Chain Management Offices (M9 building), Karl Bremer Hospital, c/o Mike Pienaar Boulevard & Frans Conradie Avenue, Bellville. Office hours: Monday to Friday, 07:30–16:00 (excluding public holidays). A soft copy on USB must also be submitted. Hard copy supersedes electronic copy if discrepancies exist. Late submissions, fax, email, or telegram submissions will not be accepted. Ensure all pages are included, signed in original black ink, and no alterations are made to the bid documents. Bidders must confirm bid document download via email to [email protected] and [email protected] with company name, contact person, phone number, and email address. Bids must be submitted on official forms provided; do not re-type or redraft. Only original, signed documents will be considered. Photocopies may be prepared for bidder records. No pages may be omitted or duplicated. Failure to submit requested information may result in disqualification. Bids submitted by security personnel or without proper authority will not be accepted. Queries about bid box location must be directed to the listed officials, not security personnel.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
14Mandatory requirement
Scope: Supply, delivery, installation, demonstration, and commissioning of blood gas analysers under a 3-year consumable placement deal for 31 Western Cape health facilities. Equipment is placed at no cost to the department; only consumables (cartridges, syringes) are procured monthly. Contractor retains ownership of equipment for the 3-year period. Facilities can adjust consumable orders monthly without penalty. Department may add facilities if need arises. Total cost of ownership must be clearly described, including cost per test.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Supported inference
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Related historical records suggest exposure; they do not prove bid contents, current capacity, or delivery.
15Mandatory requirement
Mandatory OHS Act Section 37(2) Agreement, WCBD 6.1 (B-BBEE status), and WCBD 4 (Declaration of Interests) forms must be completed.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Source: AI key requirements · requirements
Known supplier evidence
The linked award records MEDHOLD MEDICAL as appointed for this tender.
Qualified inference
Inference only
The successful bid likely addressed this expectation, but the submitted evidence and evaluation reason are unavailable.
The linked award confirms appointment only, not the submitted qualification or reason for selection.
16Mandatory requirementConflicting classification
Evaluation is based on three phases: Phase 1: Compliance with specifications, pricing, and mandatory requirements. Phase 2: 4-week trial with 3 machines at Mitchells Plain and Victoria Hospitals; evaluator report compiled. Phase 3: Final recommendation considering all inputs, followed by application of the 80:20 Preferential Procurement Points System (80 points for price, 20 points for B-BBEE). Only the B-BBEE status declared on the WCBD 6.1 form is considered. Cost per test (including all relevant costs) and real-world functionality experiences are key factors. Non-compliant bidders will be notified after the bid process concludes.
Threshold: 80 points
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Conflicting evidence
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Relevant records disagree; review the cited sources and dates.
17Mandatory requirementConflicting classification
Evaluation occurs in three phases: Phase 1: Compliance with specifications, pricing, and all mandatory requirements. Phase 2: 4-week trial with 3 machines at Mitchells Plain and Victoria Hospitals; evaluator report compiled. Phase 3: Final recommendation considering all inputs, followed by application of the 80:20 Preferential Procurement Points System (80 points for price, 20 points for B-BBEE). Only the B-BBEE status declared on the WCBD 6.1 form is considered for evaluation. Cost per test (including all relevant costs such as maintenance, consumables, and syringes) and real-world functionality experiences are key factors. Non-compliant bidders will be notified after the bid process concludes. The Department reserves the right to award the bid in part or in whole based on compliance, clinical acceptability, price, and preference points.
Threshold: 80 points
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.
Tenders-SA records other appointments with overlapping scope terms for MEDHOLD MEDICAL.
Qualified inference
Conflicting evidence
The recorded history supports exposure to related scope, but does not establish the bid evidence submitted or current delivery capacity.
Relevant records disagree; review the cited sources and dates.
18Mandatory requirement
Mandatory: CSD registration (www.csd.gov.za) at bid closing; tax compliance must be verifiable via CSD (7-day grace period if non-compliant). Submit valid SAHPRA licence as manufacturer, distributor, or wholesaler of medical devices/IVDs (no proof of application accepted). ISO 13485 certification for each manufacturer whose products are bid. OHS Act Section 37(2) Agreement (mandatory for all procurements with on-site work or health & safety risks). B-BBEE status must be declared via WCBD 6.1 form (only this applies; not CSD status). Complete WCBD 4 (Declaration of Interests, Bidders Past SCM Practices, and Independent Bid Determination). All mandatory documents on CSD/Western Cape Supplier Evidence Bank accepted. Foreign suppliers: Provide proof of SA representation if applicable. No bids from state employees or entities with state-employed directors/members. Proof of authority to sign bids required. Tax Compliance Status (TCS) PIN or printed TCS certificate must be submitted. For consortia/joint ventures/sub-contractors, each party must submit separate TCS certificate and CSD number. Bidders must ensure compliance with their tax obligations. Contract governed by General Conditions of Contract (GCC) and Special Conditions of Contract (SCC), with SCC prevailing in conflicts.
Why it matters: The source identifies this as a mandatory or eligibility condition for a compliant bid.
No source document identifier is stored for this item.