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SBL.PRP.3 Kit

by Blisscare, S.L.U.

Ref SBL.PRP.3 KIT

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8437030353SBL.PRP.3KITKD Basic UDI-DI 08437030353141UDI-DIDate2 Jun 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  • Withdrawn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
SBL.PRP.3 KIT
Primary DI / UDI-DI
08437030353141
Basic UDI-DI
8437030353SBL.PRP.3KITKD
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class IIb
Medical Purpose
Dispositivo médico para la preparación de P.R.P. (Plasma Rico en Plaquetas) autólogo. Aceleración de los procesos de curación y cicatrización del tejido conectivo y del tejido huesocartílago

Manufacturer details

EUDAMED SRN
ES-PR-000054015

Properties

  • Sterile