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Foam Pad, Adhesive Aliplast 1/8, 655S

EUDAMED

Class I (EU MDR)

Ref Z998025Model 655

by Becker Orthopedic Appliance Company

Identity

Trade Name
Foam Pad, Adhesive Aliplast 1/8, 655S EUDAMED
Device Name
Plantar/Dorsiflexion Motion Control Limiter EUDAMED
Model / Reference
655 EUDAMED
Z998025 EUDAMED

Identifiers

Primary DI / UDI-DI
00194545115333 EUDAMED
Basic UDI-DI
194545655R6 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

Foam Pad, Adhesive Aliplast 1/8, 655S by Becker Orthopedic Appliance Company — 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
US-MF-000004002
Authorised Representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Sources (1)

  • EUDAMED fe2cb094-f867-450e-b132-d96546eb134a 61 fields · synced Jun 18, 2026