Skip to content

Vacusera

by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. 15 variants

Ref 237112

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 Number++M712237PRPKITNP Basic UDI-DI +M71223711214UDI-DIDate19 Nov 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Vacusera Prp Kit
Model / Reference
237112
Primary DI / UDI-DI
+M71223711214
Basic UDI-DI
++M712237PRPKITNP
EMDN Code
B010202 Platelets concentrate transfer bags and kits
Device Class
Class III
Medical Purpose
VACUSERA® PRP Kit contains tubes and necessary accessories to be used for blood collection, transport and processing and for preparation and injection of platelet rich plasma during autologous PRP application in the clinical environment.

Manufacturer details

EUDAMED SRN
TR-PR-000050420

Other devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş.

See all devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. →

Properties

Other properties (1)

  • Sterile: No