Singapore HSA registration DE0507736
Medos Latarjet EXPERIENCE Instability Shoulder System
Device classification
- Device Class
- CLASS C
- Medical Speciality Area
- General & Plastic Surgery
Registration information
- Registration Number
- DE0507736
- Registration Date
- February 03, 2023
- Change Notification Approval Date
- April 17, 2025
- Retention Due Date
- February 02, 2026
Product description
The Latarjet EXPERIENCE is intended to provide the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries
Product Owner
- Short Name
- Medos International SARL
- Address
- Chemin-Blanc 38, CH 2400, Le locle, SWITZERLAND
Registrant
- Address
- 2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222
Importer
- Address
- 2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222 2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222
Model information
- Model Name(s)
- Latarjet EXPERIENCE Instability Shoulder System - Coracoid Drill Latarjet EXPERIENCE Instability Shoulder System - Coracoid Top Hat Drill Latarjet EXPERIENCE Instability Shoulder System - Glenoid K-Wire (380mm) Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 28mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 30mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 32mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 34mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 36mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 38mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 40mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 42mm Latarjet EXPERIENCE Screw, Titanium Sterile Screw, 44mm Latarjet EXPERIENCE Top Hat Latarjet EXPERIENCE Instability Shoulder System Latarjet EXPERIENCE Instability Shoulder System - Bristow Procedure Kit
- Model Identifier(s)
- 288201 288202 288207 288222 288223 288224 288225 288226 288227 288228 288229 288230 288231 288238 288239
About this record
Access comprehensive regulatory information for Medos Latarjet EXPERIENCE Instability Shoulder System in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0507736 and owned by Medos International SARL. The device was registered on February 03, 2023.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS C