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Conwell

EUDAMED

Class I (EU MDR)

Ref 5710 Knee Stabilizer with Silicone Pad (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
5710 Knee Stabilizer with Silicone Pad (XL) EUDAMED

Identifiers

Primary DI / UDI-DI
04719878934398 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

Yes

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 956f2757-30ed-4f56-86a3-e9a58365e2f6 61 fields · synced May 23, 2026