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PG I Rapid Quantitative Test (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref BT0505301

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
PG I Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Device Name
PG I Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
BT0505301 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260206971 EUDAMED
Basic UDI-DI
B-06933260206971 EUDAMED
EMDN Code
W0102039099 TUMOUR MARKERS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Category: Preferentially expressed antigen in melanoma (PRAME) IVD, antibody

PG I Rapid Quantitative Test (Chemiluminescence Immunoassay) by Xiamen Biotime Biotechnology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Similar devices

Also classified as Preferentially expressed antigen in melanoma (PRAME) IVD, antibody.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000012852
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (2)

  • EUDAMED 2b05ca71-b2b3-451b-b6ff-f8bb139da13c 61 fields · synced Jun 19, 2026
  • EUDAMED 422db660-bd95-48ea-aaf9-1a4da58c6542 61 fields · synced Jun 19, 2026