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Diathermy forceps bipolar, curved

EUDAMED

Class IIb (EU MDR)

Ref VE203902Model MD0105.135 Diathermy Forceps Reusable

by Oertli Instrumente AG

Identity

Trade Name
Diathermy forceps bipolar, curved EUDAMED
Model / Reference
MD0105.135 Diathermy Forceps Reusable EUDAMED
VE203902 EUDAMED

Identifiers

Primary DI / UDI-DI
07630003900590 EUDAMED
Basic UDI-DI
76300039MD0105135VE EUDAMED
Direct Marketing DI
07630003900590 EUDAMED
EMDN Code
Q020699 PHACOEMULSIFICATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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

Diathermy forceps bipolar, curved by Oertli Instrumente Ag — Class IIb — 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

EUDAMED SRN
CH-MF-000016175
Authorised Representative
Oertli Ophthalmedic Österreich GmbH AT-AR-000003554

Sources (1)

  • EUDAMED fb626078-8bd9-4676-8fe1-10d1a22c3ed7 61 fields · synced Jun 17, 2026