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THD Slide

by Thd S.P.A. 2 variants

Ref 800066FILModel THD Slide

THD Slide (800066FIL) is a Class III device made by Thd S.P.A., registered in EUDAMED on 6 Jul 2023 (Basic UDI-DI 803373771SLIDESYS00028R), 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 Number803373771SLIDESYS00028R Basic UDI-DI 18033737711009UDI-DIDate6 Jul 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
THD Slide, 800066FIL
Primary DI / UDI-DI
18033737711009
Basic UDI-DI
803373771SLIDESYS00028R
EMDN code
Z12020604 Ultrasonic proctoscopes
Device class
Class III
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
The THD Slide is to be used by physicians to perform the Transanal Doppler-guided ligation of the terminal branches of the superior haemorrhoidal artery, for the treatment of haemorrhoidal disease

Manufacturer details

EUDAMED SRN
IT-PR-000029428

Similar devices in this category

Other devices filed under LOWER GASTROINTESTINAL TRACT ENDOSCOPY INSTRUMENTS.

Other devices from Thd S.P.A.

See all devices from Thd S.P.A. →

Properties

Other properties (2, all answered No)