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Tilidin Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref TLD-U11 TLD-U23Model TLD-U11, TLD-U23

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

Identity

Trade Name
Tilidin Rapid Test EUDAMED
Device Name
Tilidin Rapid Test EUDAMED
Model / Reference
TLD-U11, TLD-U23 EUDAMED
TLD-U11 TLD-U23 EUDAMED

Identifiers

Primary DI / UDI-DI
06952804817534 EUDAMED
Basic UDI-DI
B-06952804817534 EUDAMED
EMDN Code
W0102090199 DRUGS OF ABUSE - OTHER 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

Tilidin Rapid Test by Assure Tech. (hangzhou) 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-000002170
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 1d07643a-4a86-4895-9c35-a0b6991910fa 61 fields · synced Jun 18, 2026