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VivereX™

EUDAMED

Class IIb (EU MDR)

Ref PDI600226Model VivereX™ Dressing FC 16x31

by Sunmedic AB

Identity

Trade Name
VivereX™ EUDAMED
Device Name
VivereX™ NPWT Dressing EUDAMED
Model / Reference
VivereX™ Dressing FC 16x31 EUDAMED
PDI600226 EUDAMED

Identifiers

Primary DI / UDI-DI
17350127832269 EUDAMED
Basic UDI-DI
B-17350127832269 EUDAMED
EMDN Code
M04040702 SILICONE DRESSINGS, COMBINED WITH OTHER SUBSTANCES 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

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

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 1dec12d4-47b0-45bf-96a6-d387bb798bdc 61 fields · synced Jun 18, 2026