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Venoline FAS

EUDAMED

Class I (EU MDR)

Ref VN701DMS

by Inverdia AB

Identity

Trade Name
Venoline FAS EUDAMED
Device Name
Venoline FAS AD EUDAMED
Model / Reference
VN701DMS EUDAMED

Identifiers

Primary DI / UDI-DI
07331004701048 EUDAMED
Basic UDI-DI
73310047010JG EUDAMED
Direct Marketing DI
07331004701048 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 9f2685a6-2770-482c-9103-03ce0be952af 61 fields · synced Jun 18, 2026