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BioCLIA Sample Diluent I

EUDAMED

Class A (EU MDR)

Ref MY00965Model Sample Diluent I, System Wash Buffer,System Substrate

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Sample Diluent I EUDAMED
Device Name
BioCLIA Sample Diluent I,BioCLIA System Wash Buffer,BioCLIA System Substrate EUDAMED
Model / Reference
Sample Diluent I, System Wash Buffer,System Substrate EUDAMED
MY00965 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030405274 EUDAMED
Basic UDI-DI
6924030BioCLIACR4E EUDAMED
Direct Marketing DI
06924030405274 EUDAMED
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

New Device

No

EUDAMED

BioCLIA Sample Diluent I by HOB Biotech Group Corp., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

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

Sources (1)

  • EUDAMED d10a1e81-ee92-435b-a10f-d001e66f15fe 61 fields · synced Jul 14, 2026