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Lipocube

by Stemc Bi̇yoteknoloji̇ Anoni̇m Şi̇rketi̇ 2 variants

Ref BLSVF-K/KDT

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 Number8681877009PPSX Basic UDI-DI 08681877009703UDI-DIDate30 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Adipose Tissue Procedure Pack
Model / Reference
BLSVF-K/KDT
Primary DI / UDI-DI
08681877009703
Basic UDI-DI
8681877009PPSX
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIb
Medical Purpose
The Procedure Pack is a procedural pack containing the materials required for harvesting, washing, and reinjecting adipose tissue from the patient.

Manufacturer details

EUDAMED SRN
TR-PR-000016187

Other devices from Stemc Bi̇yoteknoloji̇ Anoni̇m Şi̇rketi̇

Properties

Other properties (1)

  • Sterile: No