← Back to catalogue

Fibrin/fibrinogen Degradation Products Chemiluminescence Immunoassay Kit

EUDAMED

Class IVD General (EU MDR)

Ref S2018E-100

by Sansure Biotech Inc.

Identity

Device Name
Fibrin/fibrinogen Degradation Products Chemiluminescence Immunoassay Kit EUDAMED
Model / Reference
S2018E-100 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792737334 EUDAMED
Basic UDI-DI
B-06955792737334 EUDAMED
EMDN Code
W0103020502 FIBRINOGEN DEGRADATION PRODUCTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

Fibrin/fibrinogen Degradation Products Chemiluminescence Immunoassay Kit by Sansure Biotech Inc. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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

Manufacturer

EUDAMED SRN
CN-MF-000011392
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED ffb56d46-a408-40e7-b952-6196b52d85d7 61 fields · synced Oct 7, 2026