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Pega® Combi Line S

EUDAMED

Class IIa (EU MDR)

Ref 10521S

by Venner Medical (Deutschland) GmbH

Identity

Trade Name
PEGA® COMBI LINE S EUDAMED
PEGA COMBI LINE S EUDAMED
Device Name
PEGA® COMBI LINE S EUDAMED
PEGA® COMBI LINE EUDAMED
Model / Reference
10521S EUDAMED

Identifiers

Primary DI / UDI-DI
04260537490057 EUDAMED
Basic UDI-DI
42605374910521SFS EUDAMED
426053749PCMB017G 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 S 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 (2)

  • EUDAMED 1b9cd418-1d97-40bc-a0df-3a89553b913f 61 fields · synced Oct 6, 2026
  • EUDAMED a7ac1a39-cc91-4468-ae98-62ca7aa76451 61 fields · synced Jul 19, 2026