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VivereX™

EUDAMED

Class IIb (EU MDR)

Ref PDI600123Model VivereX™ Pump + 2 FC Dressings 10x40

by Sunmedic AB

Identity

Trade Name
VivereX™ EUDAMED
Device Name
VivereX™ NPWT System EUDAMED
Model / Reference
VivereX™ Pump + 2 FC Dressings 10x40 EUDAMED
PDI600123 EUDAMED

Identifiers

Primary DI / UDI-DI
27350127831238 EUDAMED
Basic UDI-DI
B-27350127831238 EUDAMED
EMDN Code
M04040702,Z12019003 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 c3c9e419-4a6a-4f3d-96b2-c76babe6ca54 61 fields · synced Jun 18, 2026