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General Eye Surgical Procedure Pack

by Opti̇mal Sağlik Ürün. San. Ve Diş Ti̇c. Ltd. Şti̇.

Ref 2490 4501

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699243161450 Basic UDI-DI 08699243161450UDI-DIDate11 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  • Withdrawn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

Model / Reference
2490 4501
Primary DI / UDI-DI
08699243161450
Basic UDI-DI
B-08699243161450
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TR-MF-000021855

Other devices from Opti̇mal Sağlik Ürün. San. Ve Diş Ti̇c. Ltd. Şti̇.

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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