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Tricell PRP

EUDAMED

Class IIa (EU MDR)

Ref Tricell PRP KitModel Maxxi PRP

by REV-MED Inc.

Identity

Trade Name
Tricell PRP EUDAMED
Device Name
Blood Separation Kit EUDAMED
Model / Reference
Maxxi PRP EUDAMED
Tricell PRP Kit EUDAMED

Identifiers

Primary DI / UDI-DI
08809326581178 EUDAMED
Basic UDI-DI
B-08809326581178 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 Consulting GmbH DE-AR-000045915

Sources (1)

  • EUDAMED 1071371d-181f-448e-b74f-1502870a6b51 61 fields · synced Jun 18, 2026