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Mycobacterium Tuberculosis Isoniazid Resistance Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref 32 tests/kit Model 32 tests/kit

by CapitalBio Technology (Chengdu) Co., Ltd.

Identity

Device Name
Mycobacterium Tuberculosis Isoniazid Resistance Detection Kit EUDAMED
Model / Reference
32 tests/kit EUDAMED

Identifiers

Primary DI / UDI-DI
06972221451210 EUDAMED
Basic UDI-DI
B-06972221451210 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

Mycobacterium Tuberculosis Isoniazid Resistance Detection 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

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Manufacturer

EUDAMED SRN
CN-MF-000027694
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 787d2dc1-f9c3-49f4-a8fb-817f2f5fdf07 61 fields · synced Jul 14, 2026