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Hasa Optix

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 551199

by Hasa Optix

Identity

Trade Name
HASA OPTIX EUDAMED
Sterile,Single Use,Kelman-Mcpherson LensForceps,Angled Shafts,Flat Handle,105mm FDA UDI
Generic Name
Intraocular lens folder FDA UDI
Device Name
551199x10: Sterile, Single Use, Kelman-Mcpherson Lens Forceps, Angled Shafts, Flat Handle, 105mm EUDAMED
Model / Reference
551199 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05404027417004 EUDAMEDFDA UDI
Basic UDI-DI
B-05404027417004 EUDAMED
FDA Product Code
HNR FDA UDI
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED
GMDN Term
Intraocular lens folder FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Hasa Optix by Hasa Optix — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hasa Optix
EUDAMED SRN
BE-MF-000028219

Sources (2)

  • EUDAMED 5ae5c553-1934-4f76-8d57-37e0d0ce796b 61 fields · synced Sep 18, 2026
  • FDA UDI 91fa2d7a-23c5-48de-a1aa-a00945ee95cb 34 fields · synced May 30, 2026