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VivereX™ NPWT Pump

EUDAMED

Class IIa (EU MDR)

Ref PDI600100Model VivereX™ Pump

by Sunmedic AB

Identity

Trade Name
VivereX™ NPWT Pump EUDAMED
Device Name
VivereX™ NPWT PUMP EUDAMED
Model / Reference
VivereX™ Pump EUDAMED
PDI600100 EUDAMED

Identifiers

Primary DI / UDI-DI
17350127831002 EUDAMED
Basic UDI-DI
B-17350127831002 EUDAMED
EMDN Code
Z12019003 WOUND TREATMENT EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

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™ NPWT Pump by Sunmedic AB — Class IIa — 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 91ee21cd-13e0-4b90-9633-e6f69af11673 61 fields · synced Oct 6, 2026