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Hasa Optix

by Hasa Optix 98 variants

Ref 551001

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number05404027415239 UDI-DI Date13 Nov 2023ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDD EUDAMED NumberB-05404027415239 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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Hasa Optix EUDAMED
Sterile,Single Use,Toothed Forceps,Straight Shafts,Flat Handle,85mm,1x2Teeth GUDID
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use
Device Name
551001x10: Sterile, Single Use, Toothed Forceps, Straight Shafts With 5mm Tying Platforms, Flat Handle, 85mm, 0.12mm, 1×2 Teeth
551001: Sterile, Single Use, Toothed Forceps, Straight Shafts With 5mm Tying Platforms, Flat Handle, 85mm, 0.12mm, 1×2 Teeth
Model / Reference
551001
Primary DI / UDI-DI
05404027415239, 05404027400402
Basic UDI-DI
B-05404027415239, B-05404027400402
FDA Product Code
HNR
EMDN Code
Q021102 Ophthalmic surgery forceps, single-use
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
886.4350
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
BE-MF-000028219

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Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (16)

  • 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No