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ProSet Perfusor® Set

by B. Braun Melsungen AG 2 variants

Ref 4187903

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number403923900000206427 Basic UDI-DI 04045928009588UDI-DIDate28 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ProSet Multipacks, IIa
Model / Reference
4187903
Primary DI / UDI-DI
04045928009588
Basic UDI-DI
403923900000206427
EMDN Code
A030499 Administration kits - other
Device Class
Class IIa
Medical Purpose
Multipack for drug admixture

Manufacturer details

EUDAMED SRN
DE-PR-000005115

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Properties

  • Sterile