THD Slide ENV

Primary DI

08033737711477

Basic UDI-DI Code

803373771SLIDEESYS0001BE

Reference

800168

Device Types

None provided

Regulation

Eu Mdr

Classification

Eu Md Class 3

Status

On The Market

The kit for transanal haemorrhoidal dearterialisation, includes a single use device for the operation, a sledge, a knot-pusher and a needle holder*. All in sterile and disposable packaging. The disposable device is shaped so to be introduced into the anal cavity. Its handle can lodge the optical fibre tip which shall be connected to the optical fibre cable. The THD device has on its side the lodge for the Doppler probe and a window which allowed the ligation. A slot on the side of the allow part accommodates the Doppler transducer, immediately proximal to a slit through which the stitch is applied. The knot pusher features a tiny groove at the tip to catch the thread and help tightening the knot. The moving part on the anoscope (sledge) allows a wider operating field and allows an optimal performance on the pexy. The THD SLIDE shall be only used with the THD REVOLUTION electro-medical device, which is specifically designed to detect the terminal branches of the Superior Haemorrhoidal Artery. To connect the THD SLIDE to the THD REVOLUTION refer to the THD REVOLUTION user manual.

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.

Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDR).