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Joint Body, A725-M

EUDAMED

Class I (EU MDR)

Ref A725-M2Model Standard Action Ankle Components

by Becker Orthopedic Appliance Company

Identity

Trade Name
Joint Body, A725-M EUDAMED
Device Name
Standard Action Ankle Components EUDAMED
Model / Reference
Standard Action Ankle Components EUDAMED
A725-M2 EUDAMED

Identifiers

Primary DI / UDI-DI
00194545093464 EUDAMED
Basic UDI-DI
194545STDACTANKLEZ9 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

Joint Body, A725-M 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 3c42663d-99cb-4223-ba37-1eeed85e8cf1 61 fields · synced Jun 17, 2026