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Rapid Zolpidem Test

EUDAMED

Class IVD General (EU MDR)

Ref 1L83C3-1-EU, 1L83C3-25-EU, 1L83S3-1-EU, 1L83S3-50-EU

by Xiamen Boson Biotech Co., Ltd.

Identity

Trade Name
Rapid Zolpidem Test EUDAMED
Device Name
Rapid Zolpidem Test EUDAMED
Model / Reference
1L83C3-1-EU, 1L83C3-25-EU, 1L83S3-1-EU, 1L83S3-50-EU EUDAMED

Identifiers

Primary DI / UDI-DI
D-1L83EB EUDAMED
Basic UDI-DI
B-1L83EB EUDAMED
EMDN Code
W0102160599 DRUGS OF ABUSE/TOXICOLOGY RT & POC - OTHER 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

Rapid Zolpidem Test by Xiamen Boson 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-000001096
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (2)

  • EUDAMED bd7e867c-6d19-4be7-88d3-62dec879f1b0 61 fields · synced Jul 13, 2026
  • EUDAMED bd7e867c-6d19-4be7-88d3-62dec879f1b0-1 61 fields · synced Jun 10, 2026