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Tischler Forceps

EUDAMED

Class I (EU MDR)

Ref G0700

by Gynemed

Identity

Trade Name
Tischler Forceps EUDAMED
Device Name
FOREIGN BODY MATHIEU FORCEPS, 265MM EUDAMED
Model / Reference
G0700 EUDAMED

Identifiers

Primary DI / UDI-DI
89640048540648 EUDAMED
Basic UDI-DI
8964004854gynecologyJ3 EUDAMED
EMDN Code
L05090301 GYNECOLOGICAL BIOPSY FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Tischler Forceps by Gynemed — Class I — 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
Gynemed
EUDAMED SRN
PK-MF-000042135
Authorised Representative
KHANG BAO INTERNATIONAL KFT HU-AR-000034102

Sources (1)

  • EUDAMED 08630e4c-d973-4ae1-a574-f79d53de9dd7 61 fields · synced Jun 17, 2026