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Ff-4

EUDAMED

Class I (EU MDR)

Ref 104531GR

by Endocarts International Limited

Identity

Trade Name
FF-4 EUDAMED
Device Name
Endoscopy Cart EUDAMED
Model / Reference
104531GR EUDAMED

Identifiers

Primary DI / UDI-DI
05060671730274 EUDAMED
Basic UDI-DI
506067173ENDC000001RM EUDAMED
Direct Marketing DI
05060671730274 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Category: Device sterilization/disinfection container, reusable

Ff-4 by Endocarts International Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
GB-MF-000004309
Authorised Representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Sources (1)

  • EUDAMED a5b22a97-e01e-482e-8a1a-b6e97ce7cc8e 61 fields · synced Jul 17, 2026