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Analdehner Silikon Gr.1 4x 10x L 75 mm

by medesign I.C. GmbH 2 variants

Ref MED1000747

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number425020120482Z5 Basic UDI-DI 04250201204820UDI-DIDate27 May 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
MED1000747
Primary DI / UDI-DI
04250201204820
Basic UDI-DI
425020120482Z5
EMDN Code
L06050199 Non-endoscopic urological dilation instruments, reusable - other
Device Class
Class I
Medical Purpose
Zur konservativen Therapie von Analverengung.

Manufacturer details

EUDAMED SRN
DE-PR-000040872

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Properties

Other properties (1)

  • Sterile: No