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Hasa Optix

by Hasa Optix 1,000+ variants

Ref 551007

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05404027415291 Basic UDI-DI Date25 Jan 2023RegisteredStatusActive

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  • Withdrawn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

Device Name
551007x10: Sterile, Single Use, Toothed Forceps, Straight Shafts With 5mm Tying Platforms, Flat Handle, 105mm, 0.12mm, 1×2 Teeth
551007: Sterile, Single Use, Toothed Forceps, Straight Shafts With 5mm Tying Platforms, Flat Handle, 105mm, 0.12mm, 1×2 Teeth
Model / Reference
551007
Primary DI / UDI-DI
05404027415291, 05404027400464
Basic UDI-DI
B-05404027415291, B-05404027400464
EMDN Code
Q021102 Ophthalmic surgery forceps, single-use
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000028219

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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