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Ecarteur Guiot Coudé

EUDAMED

Class I (EU MDR)

Ref 792513.00

by Ets Claude LASSERTEUX S.A

Identity

Trade Name
Ecarteur Guiot Coudé EUDAMED
Device Name
Ecarteur Guiot Coudé EUDAMED
Model / Reference
792513.00 EUDAMED

Identifiers

Primary DI / UDI-DI
03701675313279 EUDAMED
Basic UDI-DI
B-03701675313279 EUDAMED
EMDN Code
L149003 ENT RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ecarteur Guiot Coudé by Ets Claude LASSERTEUX S.A — Class I — 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
FR-MF-000001821

Sources (1)

  • EUDAMED 9f8fc26f-316b-46ae-b506-5af41f9b8c38 61 fields · synced Jun 19, 2026