← Back to catalogue

Bunion Separator

EUDAMED

Class I (EU MDR)

Ref 650011(S/M/UNI/White)

by Zhangpu Ortholife Rehabilitation Co., Ltd.

Identity

Trade Name
Bunion Separator EUDAMED
Device Name
Insole (Hallux valgus metatarsophalangeal orthosis and toe separator) EUDAMED
Model / Reference
650011(S/M/UNI/White) EUDAMED

Identifiers

Primary DI / UDI-DI
04719892931694 EUDAMED
Basic UDI-DI
47198728665WU 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 Separator by Zhangpu Ortholife 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

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

Manufacturer

EUDAMED SRN
CN-MF-000011447
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 06d8c5a4-324d-43c1-b6a7-bee72ff80545 61 fields · synced Jun 19, 2026