Identity
- Trade Name
- TriCell PRP EUDAMED
- Device Name
- Blood Separation Kit EUDAMED
- Model / Reference
- TriCell PRP New S EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809326581161 EUDAMED
- Basic UDI-DI
- B-08809326581161 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809326581161 | Class IIa | Active |
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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 5803b06b-2263-4f02-98c7-6abf654f1aed 61 fields · synced Jun 19, 2026