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S11223

EUDAMED

Class IIa (EU MDR)

Ref S11223

by Ophmed Co., Ltd.

Identity

Device Name
S11223 EUDAMED
Disposable Ophthalmic Forceps EUDAMED
Model / Reference
S11223 EUDAMED

Identifiers

Primary DI / UDI-DI
06974482530284 EUDAMED
Basic UDI-DI
B-06974482530284 EUDAMED
697448253S110009U EUDAMED
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE 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

S11223 by Ophmed Co., Ltd. — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ophmed Co., Ltd.
EUDAMED SRN
CN-MF-000032262
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (2)

  • EUDAMED 6b33dc89-8cc8-423d-9670-1d5733ef4e7d 61 fields · synced Jul 18, 2026
  • EUDAMED edeeddd2-9822-4183-95b0-26555377b63f 61 fields · synced May 18, 2026