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Bunion Corrector

EUDAMED

Class I (EU MDR)

Ref 650001(XL/Right/Gray&Silver)

by Orthotech Rehabilitation Co., Ltd.

Identity

Trade Name
Bunion Corrector EUDAMED
Device Name
Insole (Hallux valgus metatarsophalangeal orthosis and toe separator) EUDAMED
Model / Reference
650001(XL/Right/Gray&Silver) EUDAMED

Identifiers

Primary DI / UDI-DI
04719964463214 EUDAMED
Basic UDI-DI
47199644665WS EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Bunion Corrector by Orthotech Rehabilitation Co., Ltd. — 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

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Manufacturer

EUDAMED SRN
CN-MF-000051924
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 73380952-6f3b-412d-aba0-ea8c31b8b9d6 61 fields · synced Jun 19, 2026