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Endo diathermy tip 23G

by Oertli Instrumente AG 2 variants

Ref VE201733Model MD0105.136 Endo Diathermy Tips Reusable

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number76300039MD0105136VG Basic UDI-DI 07630003900545UDI-DIDate11 Dec 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
MD0105.136 Endo Diathermy Tips Reusable, VE201733
Primary DI / UDI-DI
07630003900545
Basic UDI-DI
76300039MD0105136VG
Direct Marketing DI
07630003900545
EMDN Code
Q020499 Vitrectomy devices - other
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CH-MF-000016175
Authorised representative
Oertli Ophthalmedic Österreich GmbH AT-AR-000003554

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: 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