Copan Specimen
Collection
Global #1 brand in swab & transport
Copan · UTM® · eSwab® · FLOQSwabs®
Laboratory & clinical supply · KSA
One SFDA-registered, Riyadh-based partner for diagnostics, specimen collection, immunoassay reagents, clinical chemistry, infection control and laboratory equipment — everything your laboratory needs, through a single accountable supply relationship.
Riyadh, Al MalazStock held locally under FEFO rotation, with 2–8 °C and −20 °C cold storage and lot-level traceability.
What Afiyatech supplies
From the swab to the result — Afiyatech supplies the products, the brands and the compliance assurance for every stage of your diagnostic process.
Global #1 brand in swab & transport
Copan · UTM® · eSwab® · FLOQSwabs®
Core lab & point-of-care tests
Kibion · Roche · Sysmex
Infectious disease, antenatal & cardiac
CTK Biotech · Acro · EcoTest · All Test
Endocrine, metabolic & antenatal panels
bioMérieux VIDAS · Green Care · Goldsite
Vacuum tubes, containers & transport
BD · Kangjian · Trustmomed · Sunway
Decontamination, protection & instruments
Anios · GV Health · BioBase · DLAB

Copan UTM®Viral and molecular transport, 3 ml, with regular or minitip FLOQSwabs®.

Copan eSwab®Liquid Amies for bacteriology — wound, genital, ear and throat.

Copan FecalSwab™Modified Cary-Blair for enteric pathogens and outbreak work.

Copan SRK®Environmental surface sampling for infection control and HVAC validation.
Afiyatech distributes established international makers rather than unbranded equivalents — see the full list by pillar.
Copan Group
Specimen collection
bioMérieux
VIDAS immunoassay
BD
Preanalytics
Roche Diagnostics
Clinical chemistry
Sysmex
Haematology
CTK Biotech
Rapid & POCT
Kibion
Urea breath testing
Goldsite
Immunoassay reagents
Anios
Disinfection
GV Health UK
Infection control
BioBase
Laboratory equipment
DLAB
Liquid handling
All brand names and marks are the property of their respective manufacturers and are shown to identify the products Afiyatech distributes.
Why your supplier choice matters more than ever
Vision 2030 transformation, mandatory SFDA registration and NUPCO centralised procurement mean the rules for laboratory supply have fundamentally changed since 2022.
Every medical device and IVD must hold current MDMA approval via a Saudi-licensed Authorised Representative. Purchasing from an unregistered source exposes your facility to regulatory risk and product liability.
The Kingdom’s SAR 25bn+ unified procurement channel covers 500+ public facilities. Participation requires verified SFDA status and a compliant local supply chain from day one.
Rapid expansion in hospitals, reference labs and polyclinics is driving demand for accreditation (CBAHI, JCI, CAP) — all of which scrutinise supply-chain compliance, lot traceability and product documentation.
Buyers increasingly favour Saudi-based partners who maintain local stock, manage expiry, respond to recalls and take ownership of post-market discipline — reducing operational risk for procurement teams.
Sources: SFDA MDMA/GHAD guidance (2026); NUPCO public data; Saudi Vision 2030 health programme.
SFDA
Device & IVD regulator
NUPCO
Unified procurement
CBAHI
Saudi accreditation
JCI
Hospital accreditation
CAP
Laboratory accreditation
Marks identify the regulator, the procurement channel and the accreditation frameworks our clients are audited against. They do not imply accreditation or endorsement of Afiyatech.
Why buy from Afiyatech
Consolidating your laboratory supply through Afiyatech doesn't just simplify procurement — it removes risk, improves compliance and frees your clinical team to focus on patients.
All products sourced via MDMA-approved routes with Authorised Representative coverage. Full documentation available at time of purchase — no compliance surprises at audit.
On-hand inventory with FEFO management, minimum shelf-life controls and rapid reorder — eliminating the import lead-time risk that disrupts clinical operations.
Lot-level tracking from purchase order to clinical use — supporting post-market surveillance, recall management and CBAHI/JCI audit requirements.
Technical support for product selection, platform compatibility checks and workflow changes — not just a catalogue. We match product to clinical need, not the other way round.
Diagnostics, reagents, specimen collection, infection control and PPE on a single purchase order — one invoice, one delivery, one reconciliation for your finance team.
Afiyatech will never substitute a product without explicit buyer approval. No catalogue-number switching, no ‘equivalent product’ replacement without IFU validation and your sign-off.
How we work
Switching laboratory products is a clinical and regulatory decision. Afiyatech runs every new product through five structured gates so your procurement and laboratory teams stay fully protected.
01
Confirm catalogue number, IFU, specimen type, test method and platform compatibility before any sample or quotation.
02
Verify SFDA registration, Authorised Representative status and current approved labelling for each SKU.
03
Run a controlled user-acceptance evaluation before standardising across departments — with your clinical team’s sign-off.
04
Set FEFO stock model, minimum remaining shelf life, reorder trigger and temperature requirements before first order.
05
Track lot numbers, manage complaints and recalls, and report field safety corrective actions on your behalf.
Our commitment: no clinical substitution, platform claim or “equivalent product” statement without product-specific evidence and your documented acceptance.
Already trusted across the Kingdom
Afiyatech has established direct commercial relationships across a diverse range of Saudi healthcare accounts — from national hospital groups to independent specialist clinics.
Account relationships shown identify selected engagements and do not imply endorsement. References and testimonials provided subject to client approval.
A structured way to start
Most clients begin with 2–3 product categories and expand over time. This plan makes the transition low-risk, controlled and fully documented from day one.
We audit your current supplier list, product usage, rejection rates and stock policy across all relevant categories. No commitment required — just a clearer picture of what consolidation could deliver.
Sample priority SKUs from 2–3 pillars. We confirm SFDA status, coordinate user-acceptance evaluation, arrange samples and agree the reorder model before any volume commitment.
Implement the approved product list with FEFO stock controls, lot traceability and training support. Set a quarterly review cadence to track performance and expand coverage.
Best starting categories: Copan specimen collection, POCT diagnostics, and vacuum blood-collection tubes — highest clinical frequency, clearest compliance pathway, fastest to validate.
Common questions
Short, direct answers to the questions procurement and laboratory managers raise first. If yours is not here, ask it on the quote form.
Six pillars covering the complete laboratory workflow: Copan specimen collection, clinical chemistry and haematology, rapid and POCT diagnostics, immunoassay analyser reagents, preanalytics (blood collection tubes and specimen containers), and infection control, PPE and laboratory equipment. The searchable catalogue lists every product with its manufacturer and availability.
Products are sourced via MDMA-approved routes with Authorised Representative coverage, and documentation is available at the time of purchase. Registration status is confirmed per SKU on every quotation, because status is product-specific and changes over time — we never ask a laboratory to take it on trust.
Afiyatech is based in Riyadh (Al Malaz) and holds local stock under FEFO rotation with minimum shelf-life controls. Items held in Riyadh are quoted at two to three working days; items brought in to order run four to six weeks. A sub-distribution network extends delivery to clinics and laboratories elsewhere in the Kingdom without the account relationship changing hands.
Yes. That is the point of consolidating: one purchase order, one invoice, one delivery and one reconciliation for your finance team, with a single named contact for the whole account.
No. Afiyatech will not substitute a product without explicit buyer approval — no catalogue-number switching and no ‘equivalent product’ replacement without IFU validation and your documented sign-off.
Most laboratories begin with two or three categories on a 30 / 60 / 90-day path: a fact base of current usage and stock policy, a pilot on priority SKUs with user-acceptance evaluation, then an approved product list with FEFO controls and a quarterly review. See the plan.
A distributor. Afiyatech Commercial Company is a Riyadh-based supply company (CR 101088142) representing international manufacturers — including as authorised distributor for Copan in Saudi Arabia. Manufacturers looking for a Saudi route should start on the For suppliers page.
Where we are
The office and stock sit in Al Malaz, Riyadh. Call, email or send a product list — quotations are answered by the same team that manages the account.
Al Malaz, RiyadhOpen directions in Google Maps
Take the first step
Send us your product list — or a photograph of the shelf. We come back within one working day with pricing, SFDA registration status per SKU and confirmed availability from Riyadh stock. No obligation to purchase.