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BIOLAS HO135 Aspire Katater

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

Ref CA0054 EMDN H90010102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08680400435644 Basic UDI-DIDate20 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
CA0054
Primary DI / UDI-DI
08680400435644
Basic UDI-DI
B-08680400435644
EMDN Code
H90010102 Synthetic glues
Device Class
Class III
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 3c2f23f6-15c6-4323-91fa-258d24cce739 61 fields · synced 25 Oct 2026