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ProSet Perifix®

by B. Braun Melsungen AG 156 variants

Ref 4455045

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number403923900000204829 Basic UDI-DI 04022495060235UDI-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  • Withdrawn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 Epidural Anesthesia, III
Model / Reference
4455045
Primary DI / UDI-DI
04022495060235
Basic UDI-DI
403923900000204829
EMDN Code
A01030102 Epidural anaesthesia needles and kits
Device Class
Class III
Medical Purpose
Set for Epidural Anesthesia

Manufacturer details

EUDAMED SRN
DE-PR-000005115

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Properties

  • Sterile