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INSTI Multiplex HIV-1/2 Syphilis Ab Test
EUDAMEDClass IVD Annex II List A (EU MDR)
Ref 90-1028-017 and 90-1028-018
Identity
- Trade Name
- INSTI Multiplex HIV-1/2 Syphilis Ab Test EUDAMED
- Device Name
- INSTI Multiplex Test CE es 50 and INSTI Multiplex Test CE es 350 EUDAMED
- Model / Reference
- 90-1028-017 and 90-1028-018 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00686597201619 EUDAMED
- Basic UDI-DI
- B-00686597201619 EUDAMED
- EMDN Code
- W0105010302,W0105030402 EUDAMED
Classification
- Device Class
- Class IVD Annex II List A EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
Yes
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
INSTI Multiplex HIV-1/2 Syphilis Ab Test by Biolytical Laboratories Inc. — Class IVD Annex II List A — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00686597201619 | Class IVD Annex II List A | Active |
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Manufacturer
- Manufacturer
- bioLytical Laboratories Inc.
- EUDAMED SRN
- CA-MF-000023304
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED 62d54645-5e95-406b-9b04-95037fa7523e 61 fields · synced Jun 18, 2026