← Back to catalogue

M.tuberculosis Drug Resistance Detection Array Kit

EUDAMED

Class IVD General (EU MDR)

Ref 12 tests/kit

by CapitalBio Technology (Chengdu) Co., Ltd.

Identity

Device Name
M.tuberculosis Drug Resistance Detection Array Kit EUDAMED
Model / Reference
12 tests/kit EUDAMED

Identifiers

Primary DI / UDI-DI
06972221450565 EUDAMED
Basic UDI-DI
B-06972221450565 EUDAMED
EMDN Code
W0105010703 MYCOBACTERIAL DETECTION BY NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

M.tuberculosis Drug Resistance Detection Array Kit by CapitalBio Technology (Chengdu) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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-000027694
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED a4d0de7f-0526-4391-8af3-e2ce6b73225c 61 fields · synced Jul 9, 2026