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BIOLAS Vasküler kapatma sistemi 5F

by Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Ref CA0106

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-08680400436160 Basic UDI-DI 08680400436160UDI-DIDate15 May 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  • Withdrawn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
Vasküler kapatma sistemi 5F
Model / Reference
CA0106
Primary DI / UDI-DI
08680400436160
Basic UDI-DI
B-08680400436160
EMDN Code
H90010102 Synthetic glues
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000027182

Other devices from Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →

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