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TriCell PRP

EUDAMED

Class IIa (EU MDR)

Ref TriCell PRP New

by REV-MED Inc.

Identity

Trade Name
TriCell PRP EUDAMED
Device Name
Blood Separation Kit EUDAMED
Model / Reference
TriCell PRP New EUDAMED

Identifiers

Primary DI / UDI-DI
08809326581154 EUDAMED
Basic UDI-DI
B-08809326581154 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

TriCell PRP by REV-MED Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
REV-MED Inc.
EUDAMED SRN
KR-MF-000026506
Authorised Representative
JaviTech e.K. DE-AR-000005875

Sources (1)

  • EUDAMED 7b91af77-53d2-4cf9-94df-8d4689f09559 61 fields · synced Jun 18, 2026