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Pro-gastrin-releasing Peptide Chemiluminescence Immunoassay Kit

EUDAMED

Class IVD General (EU MDR)

Ref S2050E-50

by Sansure Biotech Inc.

Identity

Device Name
Pro-gastrin-releasing Peptide Chemiluminescence Immunoassay Kit EUDAMED
Model / Reference
S2050E-50 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792739833 EUDAMED
Basic UDI-DI
B-06955792739833 EUDAMED
EMDN Code
W0102030121 PRO-GASTRIN-RELEASING PEPTIDE 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

Pro-gastrin-releasing Peptide 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

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Manufacturer

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

Sources (1)

  • EUDAMED d159b13e-2461-41d9-9280-eda3dadccfaf 61 fields · synced Jun 18, 2026