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Vacusera

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

Ref 238400A

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++M712238401EXHRY Basic UDI-DI +M712238400A1FUDI-DIDate18 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  • Withdrawn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 Biostimulants Exera
Model / Reference
238400A
Primary DI / UDI-DI
+M712238400A1F
Basic UDI-DI
++M712238401EXHRY
EMDN Code
B010202 Platelets concentrate transfer bags and kits
Device Class
Class III
Medical Purpose
The product is an advanced technology system that operates with biological materials derived from the patient’s own blood plasma. Its purpose is to accelerate tissue healing processes and support cellular regeneration in line with clinical requirements.

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