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VivaFoam™

EUDAMED

Class IIb (EU MDR)

Ref PDI600301Model VivaFoam™ Filler 10x7.5x3.2

by Sunmedic AB

Identity

Trade Name
VivaFoam™ EUDAMED
Device Name
VivaFoam™ Wound Filler EUDAMED
Model / Reference
VivaFoam™ Filler 10x7.5x3.2 EUDAMED
PDI600301 EUDAMED

Identifiers

Primary DI / UDI-DI
17350127833013 EUDAMED
Basic UDI-DI
B-17350127833013 EUDAMED
EMDN Code
M04040601 POLYURETHANE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

VivaFoam™ by Sunmedic AB — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Sunmedic AB
EUDAMED SRN
SE-MF-000012997

Sources (1)

  • EUDAMED 5185ba83-3560-412c-b53d-934b423970e2 61 fields · synced Oct 6, 2026