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SPB PRP 9ml

by Swiss Plasmabiotech GmbH

Ref SPB1105Model SPB PRP

Active European Union

CE MDD

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/MDD NumberB-07649988685446 Basic UDI-DI 07649988685446UDI-DIDate31 Jul 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Dispositivo Medico per Preparazione Di Plasma Ricco in Piastrine (Prp) Ad Uso Autologo
Model / Reference
SPB PRP, SPB1105
Primary DI / UDI-DI
07649988685446
Basic UDI-DI
B-07649988685446
EMDN Code
B0501 Platelet gel automatic preparation devices (excluding bags)
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CH-MF-000056919
Authorised representative
QUASER MEDICAL S.r.l. IT-AR-000022507

From the manufacturer

Manufacturer's product page: SPB Tubes

Other devices from Swiss Plasmabiotech GmbH

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No