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Hasa Optix

by Hasa Optix 1,000+ variants

Ref 856044

Hasa Optix (856044) is a Class IIa device made by Hasa Optix, registered in EUDAMED on 4 Feb 2023 (Basic UDI-DI B-05404027405810), active as of 22 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05404027405810 Basic UDI-DI Date4 Feb 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
856044: Sterile, Single Use, Vitreoretinal Forceps, Smooth Serrated, 27G, 145mm
856044x10: Sterile, Single Use, Vitreoretinal Forceps, Smooth Serrated, 27G, 145mm
Model / reference
856044
Primary DI / UDI-DI
05404027405810, 05404027420646
Basic UDI-DI
B-05404027405810, B-05404027420646
EMDN code
Q021102 Ophthalmic surgery forceps, single-use
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000028219

Similar devices in this category

Other devices filed under OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE.

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Properties

  • Supplied sterile
Other properties (11, all answered No)