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Hasa Optix

EUDAMED

Class IIa (EU MDR)

Ref 551202

by Hasa Optix

Identity

Trade Name
HASA OPTIX EUDAMED
Device Name
551202: Sterile, Single Use, Akahoshi Prechopper Forceps, Round Handle, Straight Shafts And Cross-Action, Maximum Tip Opening 3.0mm, 120mm EUDAMED
Model / Reference
551202 EUDAMED

Identifiers

Primary DI / UDI-DI
05404027402307 EUDAMED
Basic UDI-DI
B-05404027402307 EUDAMED
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Hasa Optix by Hasa Optix — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Hasa Optix
EUDAMED SRN
BE-MF-000028219

Sources (1)

  • EUDAMED b45dcce4-9491-4de8-a22d-d63b75d9b727 61 fields · synced May 22, 2026