← Back to catalogue

VivereX™

EUDAMED

Class IIb (EU MDR)

Ref PDI600422Model VivereX+™ Pump + 2 FC Dressings 10x30

by Sunmedic AB

Identity

Trade Name
VivereX™ EUDAMED
Device Name
VivereX™ NPWT System EUDAMED
Model / Reference
VivereX+™ Pump + 2 FC Dressings 10x30 EUDAMED
PDI600422 EUDAMED

Identifiers

Primary DI / UDI-DI
27350127834222 EUDAMED
Basic UDI-DI
B-27350127834222 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sunmedic AB
EUDAMED SRN
SE-MF-000012997

Sources (1)

  • EUDAMED 9047265d-b6cb-496e-8de9-7a544f9a50e3 61 fields · synced Oct 5, 2026