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Prontoderm® Mini Set

by B. Braun Medical AG 2 variants

Ref 400323

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 Number40392390000032172F Basic UDI-DI 04046955974122UDI-DIDate16 Oct 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  • Withdrawn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
Prontoderm Mini Set
Model / Reference
400323
Primary DI / UDI-DI
04046955974122
Basic UDI-DI
40392390000032172F
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
Medical Purpose
Set - Germ load reducing washing

Manufacturer details

EUDAMED SRN
CH-PR-000027323

Other devices from B. Braun Medical AG

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Properties

Other properties (1)

  • Sterile: No