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Insti Hiv-1/Hiv-2 Antibody Test

EUDAMED

Class IVD Annex II List A (EU MDR)

Ref 90-1015-008

by bioLytical Laboratories Inc.

Identity

Trade Name
INSTI HIV-1/HIV-2 ANTIBODY TEST EUDAMED
Device Name
INSTI HIV Ab Test CE cs 350 EUDAMED
Model / Reference
90-1015-008 EUDAMED

Identifiers

Primary DI / UDI-DI
00686597200391 EUDAMED
Basic UDI-DI
B-00686597200391 EUDAMED
EMDN Code
W0105030402 HIV MULTIPLE ANTIBODY 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 Hiv-1/Hiv-2 Antibody 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

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Manufacturer

EUDAMED SRN
CA-MF-000023304
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 7914e500-459d-4df5-870a-65a365fd9fde 61 fields · synced May 22, 2026