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Pega® Combi Line Y

EUDAMED

Class IIa (EU MDR)

Ref 10523Y

by Venner Medical (Deutschland) GmbH

Identity

Trade Name
PEGA® COMBI LINE Y EUDAMED
Device Name
PEGA® COMBI LINE Y EUDAMED
Model / Reference
10523Y EUDAMED

Identifiers

Primary DI / UDI-DI
04260537490071 EUDAMED
Basic UDI-DI
42605374910523YGC EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Pega® Combi Line Y by Venner Medical (Deutschland) GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005934

Sources (1)

  • EUDAMED 0ca9cf1a-e33f-483d-9ee2-d0f0762a3f09 61 fields · synced Jun 18, 2026