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Tuberculosis Rapid Test Device (Whole Blood +2 more)

EUDAMED

Class IVD General (EU MDR)

Ref TB-W23Model Device

by Assure Tech. (Hangzhou) Co., Ltd.

Identity

Trade Name
Tuberculosis Rapid Test Device (Whole Blood/Serum/Plasma) EUDAMED
Device Name
Tuberculosis Rapid Test EUDAMED
Model / Reference
Device EUDAMED
TB-W23 EUDAMED

Identifiers

Primary DI / UDI-DI
06952804810672 EUDAMED
Basic UDI-DI
B-06952804810672 EUDAMED
EMDN Code
W0105090199 BACTERIOLOGY - RT & POC - OTHER EUDAMED
Models / Variants
Whole Blood EUDAMED
Serum EUDAMED
Plasma EUDAMED

Classification

Device Class
Class IVD General 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

Tuberculosis Rapid Test Device (Whole Blood +2 more) by Assure Tech. (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-000002170
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 69906ef3-7477-4125-bf93-6a06caf49ad7 61 fields · synced Jun 11, 2026