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Folioxane Restricted

by bess pro gmbh EUDAMED

Active European Union

Ref FR050L

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000301888 Date2 Jul 2026IssuedStatusActive expires 27 Feb 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000301888 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    2 Jul 2026
    Expires
    27 Feb 2030
    Reason
    Change approved

Specification

EUDAMED

Device Name
Folioxane Restricted
Model / Reference
FR050L
Primary DI / UDI-DI
14063106101760
Basic UDI-DI
4063108FOLIOXREY8
Market of Registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000006209

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