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ProSet Ultraplex®

by B. Braun Melsungen AG 5 variants

Ref 4890505N

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number403923900000205628 Basic UDI-DI 04046961024576UDI-DIDate25 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  • Withdrawn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 PNB, IIa
Model / Reference
4890505N
Primary DI / UDI-DI
04046961024576
Basic UDI-DI
403923900000205628
EMDN Code
A010302 Plexus block needles and kits
Device Class
Class IIa
Medical Purpose
Set for Peripheral Nerve Blocks

Manufacturer details

EUDAMED SRN
DE-PR-000005115

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Properties

  • Sterile