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THD Recto Digital

by Thd S.P.A.

Ref 800327Model THD Recto Digital

THD Recto Digital (800327) is a Class I device made by Thd S.P.A., registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI 803373771DIANS0006YB), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803373771DIANS0006YB Basic UDI-DI 08051887047390UDI-DIDate21 Jul 2026RegisteredStatusActive

Official records

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  • Withdrawn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
THD Recto Digital, 800327
Primary DI / UDI-DI
08051887047390
Basic UDI-DI
803373771DIANS0006YB
EMDN code
G02060302 Rigid proctoscopes
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029427

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Properties

Other properties (14, all answered No)