← Back to catalogue

Cryptosporidium Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P221111

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
Cryptosporidium Antigen Rapid Test EUDAMED
Device Name
Cryptosporidium Antigen Rapid Test EUDAMED
Model / Reference
P221111 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698603737 EUDAMED
Basic UDI-DI
B-16972698603737 EUDAMED
EMDN Code
W0105090499 PARASITES - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

Cryptosporidium Antigen Rapid Test by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — 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-000013495
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 4a0b8785-80fb-4fd2-8575-e4a705911276 61 fields · synced Jun 18, 2026