← Back to catalogue

BioCLIA Allergy Reagent Kit, F88

EUDAMED

Class IVD General (EU MDR)

Ref MY01295Model F88, 50 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Allergy Reagent Kit, F88 EUDAMED
Device Name
BioCLIA Allergy Reagent Kit EUDAMED
Model / Reference
F88, 50 Tests/Kit EUDAMED
MY01295 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030410391 EUDAMED
Basic UDI-DI
B-06924030410391 EUDAMED
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Category: Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

BioCLIA Allergy Reagent Kit, F88 by HOB Biotech Group Corp., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000023974
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 56ed6228-5a8f-455e-b418-e314448d98c8 61 fields · synced Jul 26, 2026