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BioCLIA Allergy Reagent Kit, H1

EUDAMED

Class IVD General (EU MDR)

Ref MY01302Model H1, 50 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Allergy Reagent Kit, H1 EUDAMED
Device Name
BioCLIA Allergy Reagent Kit EUDAMED
Model / Reference
H1, 50 Tests/Kit EUDAMED
MY01302 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030410469 EUDAMED
Basic UDI-DI
B-06924030410469 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, H1 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

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Manufacturer

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

Sources (1)

  • EUDAMED e42b95b6-9682-4b5a-8f05-b2e60059c9e8 61 fields · synced Jun 19, 2026