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Pelvinity

EUDAMED

Class I (EU MDR)

Ref PELV01

by Femma

Identity

Device Name
PELVINITY EUDAMED
Model / Reference
PELV01 EUDAMED

Identifiers

Primary DI / UDI-DI
37700254260130 EUDAMED
Basic UDI-DI
3770025426PELVINITYP4 EUDAMED
Direct Marketing DI
37700254260130 EUDAMED
EMDN Code
M030499 ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER 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: Compression/pressure sock/stocking, reusable

Pelvinity by Femma — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Femma
EUDAMED SRN
FR-MF-000047433

Sources (1)

  • EUDAMED 41851494-0d68-4152-aab7-9819f7ba6024 61 fields · synced Sep 17, 2026