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PEGA® Infuse

EUDAMED

Class IIb (EU MDR)

Ref 60020

by Venner Medical (Deutschland) GmbH

Identity

Trade Name
PEGA® Infuse EUDAMED
Device Name
PEGA® Infuse Infusionspumpe EUDAMED
Model / Reference
60020 EUDAMED

Identifiers

Primary DI / UDI-DI
04260537490224 EUDAMED
Basic UDI-DI
B-04260537490224 EUDAMED
EMDN Code
Z12030301 INFUSION PUMPS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

PEGA® Infuse by Venner Medical (Deutschland) GmbH — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: Broschüre laden

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000005934

Sources (1)

  • EUDAMED af3eee6f-d1db-4551-a985-9b30df20b3cc 61 fields · synced Oct 8, 2026