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Prontosan® acute Wound Gel

by B. Braun Medical AG EUDAMED

Active European Union

Ref 400521

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40392390000009212L Basic UDI-DIDate17 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2247049TD05 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0344
    Issued
    25 Sep 2024
    Expires
    1 Sep 2029
  • 2247049CE01 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0344
    Issued
    25 Sep 2024
    Expires
    1 Oct 2028
    Reason
    Add device or group

Specification

EUDAMED

Device Name
Prontosan acute Wound Gel
Model / Reference
400521
Primary DI / UDI-DI
07612449144752
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000017781
Authorised representative
B. Braun Melsungen AG DE-AR-000000202

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