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Thd Revolution

by Thd S.P.A. 4 variants

Ref 700017

Thd Revolution (700017) is a Class IIa device made by Thd S.P.A., registered in EUDAMED on 23 Apr 2024 (Basic UDI-DI 803373771DOP0001AK), active as of 7 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803373771DOP0001AK Basic UDI-DI 08033737712887UDI-DIDate23 Apr 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
700017
Primary DI / UDI-DI
08033737712887
Basic UDI-DI
803373771DOP0001AK
EMDN code
Z12059005 Blood flow velocimeters
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029427

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR CARDIOLOGY AND CARDIAC SURGERY.

Other devices from Thd S.P.A.

See all devices from Thd S.P.A. →

Properties

  • Sterilise before use
Other properties (13, all answered No)