← Back to catalogue

Pedipro Softer

EUDAMED

Class I (EU MDR)

Ref 25600120200599Ref 25600120100599

by Thuasne

Identity

Device Name
Pedipro Softer EUDAMED
Model / Reference
25600120200599 EUDAMED
25600120100599 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790068235 EUDAMED
03111790068228 EUDAMED
Basic UDI-DI
311179FR0046AF4 EUDAMED
Direct Marketing DI
03111790068235 EUDAMED
03111790068228 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

Pedipro Softer by Thuasne — 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

Manufacturer
Thuasne
EUDAMED SRN
FR-MF-000001201

Sources (2)

  • EUDAMED af83234b-1e4b-4157-a614-f13aff71d973 61 fields · synced Jul 20, 2026
  • EUDAMED 46c24697-307f-42cf-909b-9c0845169542 61 fields · synced May 18, 2026