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Knee Support

EUDAMED

Class I (EU MDR)

Ref LB-21 Model LB-21,LB-214,LB-215,LB-216,LB-217,LB-218,LB-219,LB-220,LP-228,LP-229,LP-230,LP-231,LP-232,LP-233,LP-234,LE-238,LE-239,LE-240

by Shenzhen QiJiang Technology Co., Ltd

Identity

Device Name
Knee Support EUDAMED
Model / Reference
LB-21,LB-214,LB-215,LB-216,LB-217,LB-218,LB-219,LB-220,LP-228,LP-229,LP-230,LP-231,LP-232,LP-233,LP-234,LE-238,LE-239,LE-240 EUDAMED
LB-21 EUDAMED

Identifiers

Primary DI / UDI-DI
06979884285008 EUDAMED
Basic UDI-DI
697988428KS001V7 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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: Ankle/foot orthosis

Knee Support by Shenzhen QiJiang Technology Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000042530
Authorised Representative
REP Europe GmbH DE-AR-000025090

Sources (1)

  • EUDAMED 6549ee6f-c798-426f-b977-223c4bc93027 61 fields · synced Jun 18, 2026