← Back to catalogue

Maramed Posterior Leaf Spring Full Foot Open Heel, Medium, Left

EUDAMED

Class I (EU MDR)

Ref PLS-FFOH-200L

by BioSculptor Corporation

Identity

Trade Name
Maramed Posterior Leaf Spring Full Foot Open Heel, Medium, Left EUDAMED
Device Name
Maramed Posterior Leaf Spring AFO EUDAMED
Model / Reference
PLS-FFOH-200L EUDAMED

Identifiers

Primary DI / UDI-DI
00810050250870 EUDAMED
Basic UDI-DI
081005025PLS8X EUDAMED
Direct Marketing DI
00810050250870 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Maramed Posterior Leaf Spring Full Foot Open Heel, Medium, Left by BioSculptor Corporation — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000012686
Authorised Representative
Eurolink Europe Compliance Limited IE-AR-000002852

Sources (1)

  • EUDAMED c509f107-737a-4d99-8465-c738bef51492 61 fields · synced Aug 1, 2026