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Bimanual I/A System reusable (T)

by Bürki inno med AG Switzerland EUDAMED

Ref BAO 105/T EMDN Q0299

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764013745P02P04X4 Basic UDI-DIDate24 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
I/A System reusable
Model / Reference
BAO 105/T
Primary DI / UDI-DI
07640137450335
Basic UDI-DI
764013745P02P04X4
Direct Marketing DI
07640137450335
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000017443
Authorised representative
Bürki inno med GmbH DE-AR-000008073

From the manufacturer

Manufacturer's product page: Bimanual I/A System reusable 20G, 21G, 22G, 23G

Other devices from Bürki inno med AG

See all devices from Bürki inno med AG →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
Other properties (12)
  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 22b31848-5994-4bbb-91b0-1da280c2c325 61 fields · synced 24 Oct 2026