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ERGO-Schaftrohr

EUDAMED

Class IIa (EU MDR)

Ref 20195-241

by Erbe Elektromedizin GmbH

Identity

Trade Name
ERGO-Schaftrohr EUDAMED
Device Name
Bipolar instruments, LAP EUDAMED
Model / Reference
20195-241 EUDAMED

Identifiers

Primary DI / UDI-DI
04050147011403 EUDAMED
Basic UDI-DI
B-04050147011403 EUDAMED
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

ERGO-Schaftrohr by Erbe Elektromedizin GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000005498

Sources (1)

  • EUDAMED dc2e9c1e-5c1e-4097-8872-c5984ee1fd3a 61 fields · synced Sep 19, 2026