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Venoline FAS

EUDAMED

Class I (EU MDR)

Ref VN702XSR

by Inverdia AB

Identity

Trade Name
Venoline FAS EUDAMED
Device Name
Venoline FAS EUDAMED
Model / Reference
VN702XSR EUDAMED

Identifiers

Primary DI / UDI-DI
07331004702236 EUDAMED
Basic UDI-DI
7331004770206J EUDAMED
Direct Marketing DI
07331004702236 EUDAMED
EMDN Code
M030405 COMPRESSION STOCKINGS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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, single-use

Venoline FAS by Inverdia AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Inverdia AB
EUDAMED SRN
SE-MF-000047520

Sources (1)

  • EUDAMED 054de08c-0484-480a-8c41-5c46f6b98a28 61 fields · synced Jun 18, 2026