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Desmarres Lid Retractors

by Acheron Instruments (Private) Limited 4 variants

Ref AI-GS-05-116

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G733LIDRETRACTOR01H9 Basic UDI-DI +G733AIGS051160QUDI-DIDate21 Oct 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  • Withdrawn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
Desmarres Lid Retractors
Model / Reference
AI-GS-05-116
Primary DI / UDI-DI
+G733AIGS051160Q
Basic UDI-DI
++G733LIDRETRACTOR01H9
EMDN Code
L170102 Ocular and endocular retractors, reusable
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
PK-MF-000037497
Authorised representative
KHANG BAO INTERNATIONAL KFT HU-AR-000034102

Other devices from Acheron Instruments (Private) Limited

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Properties

  • 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