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Brucella IgG/IgM Rapid Test (WB +2 more)

EUDAMED

Class IVD General (EU MDR)

Ref Bru-4022

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Brucella IgG/IgM Rapid Test(WB/S/P) EUDAMED
Device Name
Brucella IgG/IgM Rapid Test(WB/S/P) EUDAMED
Model / Reference
Bru-4022 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646BRU001KY3J EUDAMED
Basic UDI-DI
B-697424646BRU001KY3J EUDAMED
EMDN Code
W0105090199 BACTERIOLOGY - RT & POC - OTHER EUDAMED
Models / Variants
WB EUDAMED
S EUDAMED
P EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Brucella IgG/IgM Rapid Test (WB +2 more) by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — 3 models

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
UnicareQ GmbH DE-AR-000051497

Sources (1)

  • EUDAMED eeb33d41-b27a-49c1-9ae4-70ef6d2ffe0b 61 fields · synced Jul 10, 2026