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Conwell

EUDAMED

Class I (EU MDR)

Ref 5722 Defender Mesh OA Knee Brace (Left XL)Model 5701, 5702, 5703, 5704, 5705, 5706, 5707, 5708, 5710, 57110, 57120, 5713, 5714, 57150, 57160, 5717, 57200, 5722, 5723, 5724, 5725, 57260, 5727, 5728, 5729, 57300, 57310, 57320, 57330, 57340, 5750, 5755, 5760, 5765, 57900

by Conwell Medical Co., Ltd.

Identity

Trade Name
Conwell EUDAMED
Device Name
Soft Support, Brace, Orthosis (Knee series) EUDAMED
Model / Reference
5701, 5702, 5703, 5704, 5705, 5706, 5707, 5708, 5710, 57110, 57120, 5713, 5714, 57150, 57160, 5717, 57200, 5722, 5723, 5724, 5725, 57260, 5727, 5728, 5729, 57300, 57310, 57320, 57330, 57340, 5750, 5755, 5760, 5765, 57900 EUDAMED
5722 Defender Mesh OA Knee Brace (Left XL) EUDAMED

Identifiers

Primary DI / UDI-DI
04719878934725 EUDAMED
Basic UDI-DI
471987893KNEE-5700022 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Conwell by Conwell Medical Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Conwell Medical Co., Ltd.
EUDAMED SRN
TW-MF-000012101
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 5dd0b8bf-f01c-4d95-9267-63a700378687 61 fields · synced Oct 7, 2026