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Equipo de reanimación adulto PVC U-1002D

by Stagi International SA

Ref 3240126Model U-1002D

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number30013REANIM1002D3240126NJ Basic UDI-DI 08430013211261UDI-DIDate8 Jun 2026RegisteredStatusActive

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  • Withdrawn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
Equipo de reanimación para adultos en PVC
Model / Reference
U-1002D, 3240126
Primary DI / UDI-DI
08430013211261
Basic UDI-DI
30013REANIM1002D3240126NJ
EMDN Code
R010102, R03010101, R03020201, R9099
Device Class
Class IIa
Medical Purpose
Equipo de reanimación de emergencia respiratoria

Manufacturer details

EUDAMED SRN
ES-PR-000042695

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Properties

Other properties (1)

  • Sterile: No