Bipolare Pinzette; bajonett

by Erbe Elektromedizin GmbH 24 variants

Ref 20195-002

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number4050147Bi-Forceps-RU-T6 Basic UDI-DI 04050147005426UDI-DI	Date13 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Bipolar forceps, RU
Model / Reference: 20195-002

Primary DI / UDI-DI: 04050147005426
Basic UDI-DI: 4050147Bi-Forceps-RU-T6
Direct Marketing DI: 04050147005426
EMDN Code: L180401 Open electrosurgery forceps, reusable
Models / Variants: Bipolare Pinzette
bajonett

Device Class: Class IIb
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000005498

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Class I

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No