gudid
Primary ID: THD ANOLIFT US
THD SLIDE ONE (UDI THD ANOLIFT US)
Manufactured by THD SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for THD SLIDE ONE - Primary ID THD ANOLIFT US
Technical Specifications
- Model Number
- THD ANOLIFT US
- Product Code / EMDN
- JAF
- Device Name
- THD Slide is specifically designed to be immediately used with the Revolution doppler de-arterialiser. THD Slide is a specifically designed anoscope/proctoscope for improving the THD procedure while treating the higher grades of the haemorrhoidal disease. The specific shape of the anoscope/proctoscope, which includes a sliding part, allows to perform the ligation and the prolapse reduction with the same device and reduces the disease for the patient and speeds up the procedure. The peculiar shape of the anoscope/proctoscope, with the sliding probe holder, allows to perform ligation and prolapse reduction with a single tool. The THD Slide anoscope/proctoscope is made in a clear, medical grade, plastic which allows, with the use of the shaped fibre optic tip, a perfect lightning of the operative field. The particular THD anoscope/proctoscope is designed to maintain the right strain into the anal cavity during the treatment and it presents a lodge for the THD needle holder. The supplied doppler probe lodges into the anoscope/proctosocpe and is in contact with the anal mucosa for an accurate detection of the haemorrhoidal arteries. The THD ANOLIFT US kit is a disposable kit containing the following medical devices, each one individually pack withing each kit carton box:- THD Slide- THD Doppler Probe - Sutures (both traditional for ligation and barbed sutures for mucopexy)
- Database Sync Date
- 2026-08-09 09:04:32
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of THD SLIDE ONE?
The registered manufacturer of record for THD SLIDE ONE is THD SPA.
What is the Primary UDI-DI identifier for THD SLIDE ONE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is THD ANOLIFT US.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
Other Devices by THD SPA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint