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Laminin (LN) eCLIA

EUDAMED

Class IVD General (EU MDR)

Ref 692025Model 50T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Laminin (LN) eCLIA EUDAMED
Device Name
Laminin (LN) eCLIA EUDAMED
Model / Reference
50T EUDAMED
692025 EUDAMED

Identifiers

Primary DI / UDI-DI
06970341685638 EUDAMED
Basic UDI-DI
B-06970341685638 EUDAMED
EMDN Code
W0102039006 LAMININ 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

Laminin (LN) eCLIA by Shenzhen Lifotronic Technology 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-000005654
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 2c3cc667-b305-4ed4-8418-b23feaf91c54 61 fields · synced Jun 18, 2026