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Pro-Gastrin-Releasing Peptide Assay Kit (Chemiluminescent Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref S2117E-24Ref S2117E-48

by Sansure Biotech Inc.

Identity

Device Name
Pro-Gastrin-Releasing Peptide Assay Kit (Chemiluminescent Immunoassay) EUDAMED
Model / Reference
S2117E-24 EUDAMED
S2117E-48 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792741249 EUDAMED
06955792741256 EUDAMED
Basic UDI-DI
B-06955792741249 EUDAMED
B-06955792741256 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 Assay Kit (Chemiluminescent Immunoassay) 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 (2)

  • EUDAMED 43fbbfe6-7cc4-41a0-a1ac-a262aa41448b 61 fields · synced Jul 8, 2026
  • EUDAMED 61fa92bb-28df-46e0-9899-d86455983512 61 fields · synced May 17, 2026