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4K F-Sonic 23G/30°

EUDAMED

Class IIa (EU MDR)

Ref PA603023FK

by Medicel AG

Identity

Trade Name
4K F-Sonic 23G/30° EUDAMED
Device Name
Phaco Accessories Set EUDAMED
Model / Reference
PA603023FK EUDAMED

Identifiers

Primary DI / UDI-DI
07630055240682 EUDAMED
Basic UDI-DI
076300552PASU033D EUDAMED
Direct Marketing DI
07630055240682 EUDAMED
EMDN Code
Q020699 PHACOEMULSIFICATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

4K F-Sonic 23G/30° by Medicel AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Medicel AG
EUDAMED SRN
CH-MF-000016652
Authorised Representative
Rudolf Riester GmbH DE-AR-000015844

Sources (1)

  • EUDAMED 8128dcaa-e1e2-4aae-bdbc-6250665ec77d 61 fields · synced Oct 6, 2026