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Thd Hemorflow

by Thd S.P.A.

Ref 800339Model THD HEMORFLOW

Thd Hemorflow (800339) is a Class I device made by Thd S.P.A., registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 803373771DIANS0007YD), 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 Number803373771DIANS0007YD Basic UDI-DI 08051687050019UDI-DIDate9 Oct 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  • Withdrawn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 HEMORFLOW, 800339
Primary DI / UDI-DI
08051687050019
Basic UDI-DI
803373771DIANS0007YD
EMDN code
G02060301 Anoscopes
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)