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VivereX™

EUDAMED

Class IIb (EU MDR)

Ref PDI605226Model VivereX™ MP FC 16x31

by Sunmedic AB

Identity

Trade Name
VivereX™ EUDAMED
Device Name
VivereX™ NPWT Dressing EUDAMED
Model / Reference
VivereX™ MP FC 16x31 EUDAMED
PDI605226 EUDAMED

Identifiers

Primary DI / UDI-DI
27350127832266 EUDAMED
Basic UDI-DI
B-27350127832266 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 b4bc7a76-25eb-4dd5-a73c-689c2663af5a 61 fields · synced Oct 6, 2026