Skip to content

Aniplate™ PRP & iPRF kit

by Biovico Spółka z ograniczoną odpowiedzialnością

Ref PRO00824

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5902020847ANIkit9Y Basic UDI-DI 05907381851441UDI-DIDate18 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
PRO00824
Primary DI / UDI-DI
05907381851441
Basic UDI-DI
5902020847ANIkit9Y
EMDN Code
B0599 Topical use blood components preparation devices - other
Device Class
Class IIa
Medical Purpose
The procedure pack is designed for isolation and separation of platelet-rich plasma (PRP) or platelet-rich fibrin (iPRF) from patient’s own blood.

Manufacturer details

EUDAMED SRN
PL-PR-000010561

Other devices from Biovico Spółka z ograniczoną odpowiedzialnością

See all devices from Biovico Spółka z ograniczoną odpowiedzialnością →

Properties

  • Sterile