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MiniDock MTB Test

EUDAMED

Class IVD General (EU MDR)

Ref RM1012202-10

by Guangzhou Pluslife Biotech Co., Ltd

Identity

Trade Name
MiniDock MTB Test EUDAMED
Device Name
MTB Nucleic Acid Test Card EUDAMED
Model / Reference
RM1012202-10 EUDAMED

Identifiers

Primary DI / UDI-DI
06975327120653 EUDAMED
Basic UDI-DI
B-06975327120653 EUDAMED
EMDN Code
W0105010703 MYCOBACTERIAL DETECTION BY NA REAGENTS 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

MiniDock MTB Test by Guangzhou Pluslife Biotech Co., Ltd — Class IVD General — 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
CN-MF-000025784
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 32a9248c-7c26-461c-87c7-d29237e74d90 61 fields · synced Jul 9, 2026