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Dr.PRP

EUDAMED

Class IIa (EU MDR)

Ref Dr.PRP

by Rmedica Co., Ltd

Identity

Trade Name
Dr.PRP EUDAMED
Device Name
Dr.PRP EUDAMED
Model / Reference
Dr.PRP EUDAMED

Identifiers

Primary DI / UDI-DI
88094102000608 EUDAMED
Basic UDI-DI
880941020DrPRPMB EUDAMED
EMDN Code
B0399 APHERESIS DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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

Dr.PRP by RMEDICA 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
Rmedica Co., Ltd
EUDAMED SRN
KR-MF-000023104
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 665566dd-5568-4036-b008-8c0295149151 61 fields · synced Jul 20, 2026