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PRP tube with anticoagulant

EUDAMED

Class IIa (EU MDR)

Ref EU-PRP(G)-10SModel HBH-PRP Tube-05, HBH-PRP Tube-08, HBH-PRP Tube-10, HBH-PRP Tube-12, HBH-PRP Tube-20, HBH-PRP Tube-30

by Beijing Hanbaihan Medical Devices Co., Ltd.

Identity

Device Name
PRP tube with anticoagulant EUDAMED
Model / Reference
HBH-PRP Tube-05, HBH-PRP Tube-08, HBH-PRP Tube-10, HBH-PRP Tube-12, HBH-PRP Tube-20, HBH-PRP Tube-30 EUDAMED
EU-PRP(G)-10S EUDAMED

Identifiers

Primary DI / UDI-DI
06924464103784 EUDAMED
Basic UDI-DI
69244641004TE EUDAMED
Direct Marketing DI
06924464103784 EUDAMED
EMDN Code
B030101 APHERESIS PLASMA COLLECTION DEVICES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

PRP tube with anticoagulant by Beijing Hanbaihan Medical Devices Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000028967
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 24d43bed-2419-4057-8a50-ceaeca6646dc 61 fields · synced Oct 7, 2026