← Back to catalogue

Fluorescence Immune Analyzer

EUDAMED

Class A (EU MDR)

Ref QD-S900

by Nanjing Vazyme Medical Technology Co., Ltd.

Identity

Trade Name
Fluorescence Immune Analyzer EUDAMED
Device Name
Fluorescence Immune Analyzer EUDAMED
Model / Reference
QD-S900 EUDAMED

Identifiers

Primary DI / UDI-DI
06973315734707 EUDAMED
Basic UDI-DI
6973315738668BQ EUDAMED
Direct Marketing DI
06973315734707 EUDAMED
EMDN Code
W0201020101 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Fluorescence Immune Analyzer by Nanjing Vazyme Medical Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000031032
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED affca7bc-f75c-43b5-9c23-730a71eb3bb0 61 fields · synced Jun 18, 2026