Skip to content

LDD001

by Paolo Gobbi Frattini S.r.l. Unipersonale

Ref LDD001Model LDD

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 Number805568484LDDPY Basic UDI-DI 08055684840703UDI-DIDate19 Oct 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  • Withdrawn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

Model / Reference
LDD, LDD001
Primary DI / UDI-DI
08055684840703
Basic UDI-DI
805568484LDDPY
EMDN Code
V0499 Clinical use containers (non-IVD) - other
Device Class
Class IIa
Medical Purpose
Kit LDD

Manufacturer details

EUDAMED SRN
IT-PR-000059201

Other devices from Paolo Gobbi Frattini S.r.l. Unipersonale

See all devices from Paolo Gobbi Frattini S.r.l. Unipersonale →

Properties

  • Sterile