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Set Episiotomie

by Hemodia SAS 4 variants

Ref 9860_1

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 Number3661379ASS17GYN01PB Basic UDI-DI 03661379265994UDI-DIDate8 Oct 2025RegisteredStatusActive

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  • Withdrawn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
Assemblage GYNECO OBSTETRIQUE STE
Model / Reference
9860_1
Primary DI / UDI-DI
03661379265994
Basic UDI-DI
3661379ASS17GYN01PB
EMDN Code
U1099 Obstetrics devices - other
Device Class
Class I
Medical Purpose
Les assemblages de la gamme ‘Gynéco-obstétrique’ sont destinés à : Utilisés lors d'actes et examens pendant ou en dehors de la grossesse, ainsi que pour les soins post opératoires suite à une intervention en gynécologie ou en obstétrique

Manufacturer details

EUDAMED SRN
FR-PR-000007189

Other devices from Hemodia SAS

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Properties

  • Sterile