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PRP tube without anticoagulant

EUDAMED

Class IIa (EU MDR)

Ref EU-PRF(G)-F30Model HBH-PRP Tube/N-05,HBH-PRP Tube/N -08,HBH-PRP Tube/N -10,HBH-PRP Tube/N -12,HBH-PRP Tube/N -20,HBH-PRP Tube/N -30, HBH-PRP Tube/F-05,HBH-PRP Tube/F-08,HBH-PRP Tube/F-10,HBH-PRP Tube/F-12,HBH-PRP Tube/F-20, HBH-PRP Tube/F-30

by Beijing Hanbaihan Medical Devices Co., Ltd.

Identity

Device Name
PRP tube without anticoagulant EUDAMED
Model / Reference
HBH-PRP Tube/N-05,HBH-PRP Tube/N -08,HBH-PRP Tube/N -10,HBH-PRP Tube/N -12,HBH-PRP Tube/N -20,HBH-PRP Tube/N -30, HBH-PRP Tube/F-05,HBH-PRP Tube/F-08,HBH-PRP Tube/F-10,HBH-PRP Tube/F-12,HBH-PRP Tube/F-20, HBH-PRP Tube/F-30 EUDAMED
EU-PRF(G)-F30 EUDAMED

Identifiers

Primary DI / UDI-DI
06924464103326 EUDAMED
Basic UDI-DI
69244641001T8 EUDAMED
Direct Marketing DI
06924464103326 EUDAMED
EMDN Code
B030101 APHERESIS PLASMA COLLECTION DEVICES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

No

EUDAMED

PRP tube without 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

Manufacturer
Beijing Hanbaihan Medical Devices Co., Ltd.
EUDAMED SRN
CN-MF-000028967
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 0f33789d-185a-4cc2-9d2f-779caa5842e7 61 fields · synced Jun 19, 2026