← Back to catalogue

Sprystep Footplate

EUDAMED

Class I (EU MDR)

Ref U3120460205002

by Thuasne Deutschland GmbH

Identity

Device Name
SPRYSTEP FOOTPLATE EUDAMED
Model / Reference
U3120460205002 EUDAMED

Identifiers

Primary DI / UDI-DI
04035459415347 EUDAMED
Basic UDI-DI
4035459DE0905F4V EUDAMED
Direct Marketing DI
04035459415347 EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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: Orthotic insole, prefabricated, non-antimicrobial

Sprystep Footplate by Thuasne Deutschland GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

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
DE-MF-000006210

Sources (1)

  • EUDAMED 79c56605-2a0a-45a1-a87e-bad387180558 61 fields · synced Jun 18, 2026