Singapore HSA registration DE0014315
Ad Rem Technology Veinoplus V.I. Model 2.1
Device classification
- Device Class
- CLASS B
- Medical Speciality Area
- General Hospital
- HSA Product Code
- HSAMDB00104
- HS Code
- 90191010
Registration information
- Registration Number
- DE0014315
- Registration Date
- November 15, 2013
- Change Notification Approval Date
- May 25, 2023
- Retention Due Date
- November 14, 2025
Product description
Veinoplus® V.I. model 2.1 is an electro-muscular stimulator that causes contractions by electrically stimulating the calf muscles by means of Veinoplus® pack electrodes. Veinoplus VI is indicated for: increase of blood circulation, improvement of venous return, pain reduction and reduction of leg swelling (oedema) of venous origin.
Product Owner
- Short Name
- Ad Rem Technology
- Address
- 162, rue du Faubourg Saint Honore, 75008 Paris, FRANCE
Registrant
- Name
- TOPMED PTE. LTD.
- Address
- 10 BUKIT BATOK CRESCENT, THE SPIRE, #10-02, SINGAPORE 658079
Importer
- Address
- 23 NEW INDUSTRIAL ROAD, SOLSTICE BUSINESS CENTER, #03-08, SINGAPORE 536209
Model information
- Model Name(s)
- Veinoplus V.I. Model 2.1 Veinoplus PACK
- Model Identifier(s)
- 3401048883186 8x13 OVAL
About this record
Access comprehensive regulatory information for Ad Rem Technology Veinoplus V.I. Model 2.1 in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0014315 and owned by Ad Rem Technology. The device was registered on November 15, 2013.
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 B