Skip to content

Set Amnioscopio Completo

by Gima SpA

Ref 29970

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8023279000000000E1CC000VK Basic UDI-DI 08023279299700UDI-DIDate10 Jun 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
Set Amnioscopio Completo
Model / Reference
29970
Primary DI / UDI-DI
08023279299700
Basic UDI-DI
8023279000000000E1CC000VK
EMDN Code
Z12029085 Various instruments for endoscopy and mini-invasive surgery - consumables
Device Class
Class I
Medical Purpose
SET AMNIOSCOPIO

Manufacturer details

EUDAMED SRN
IT-PR-000034105

Other devices from Gima SpA

See all devices from Gima SpA →

Properties

Other properties (1)

  • Sterile: No