← Back to catalogue

Redresseur hallux valgus TG

EUDAMED

Class I (EU MDR)

Ref 6800-G

by Gibaud

Identity

Trade Name
Redresseur hallux valgus TG EUDAMED
Device Name
Redresseur hallux valgus EUDAMED
Model / Reference
6800-G EUDAMED

Identifiers

Primary DI / UDI-DI
03322541065667 EUDAMED
Basic UDI-DI
332254066L4 EUDAMED
Direct Marketing DI
03322541065667 EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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: Orthotic insole, prefabricated, non-antimicrobial

Redresseur hallux valgus TG by Gibaud — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Gibaud
EUDAMED SRN
FR-MF-000014279

Sources (1)

  • EUDAMED a6f1f784-fd2b-4242-bcfa-3b5ae967de3b 61 fields · synced Jun 18, 2026