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ProSet Certofix® Quinto

by B. Braun Melsungen AG 6 variants

Ref 4167024S

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 Number40392390000020582C Basic UDI-DI 04046964216626UDI-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  • Withdrawn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 CVC Sets, III
Model / Reference
4167024S
Primary DI / UDI-DI
04046964216626
Basic UDI-DI
40392390000020582C
EMDN Code
C010299 Central venous catheters - other
Device Class
Class III
Medical Purpose
Set for Central Venous Catheterization

Manufacturer details

EUDAMED SRN
DE-PR-000005115

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Properties

  • Sterile