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Pro Shield Pneumatic Walker

EUDAMED

Class I (EU MDR)

Ref MWKUP03 (L/UNI/BK/17)Model Walker Boot Series

by e-life International Co., Ltd.

Identity

Trade Name
Pro Shield Pneumatic Walker EUDAMED
Device Name
Ankle/foot orthosis EUDAMED
Model / Reference
Walker Boot Series EUDAMED
MWKUP03 (L/UNI/BK/17) EUDAMED

Identifiers

Primary DI / UDI-DI
04712302989230 EUDAMED
Basic UDI-DI
471230298WKS2 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Pro Shield Pneumatic Walker by e-life International 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
TW-MF-000009901
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 2e048b90-52b1-4d5e-9bcd-2f276f4ac1b5 61 fields · synced Oct 9, 2026