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Ad Rem Technology Veinoplus V.I. Model 2.1 - HSA Registration DE0014315

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.

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CLASS B
DE0014315
Ad Rem Technology Veinoplus V.I. Model 2.1
HSA Registration Number: DE0014315
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Product Description

Veinoplusยฎ V.I. model 2.1 is an electro-muscular stimulator that causes contractions by electrically stimulating the calf muscles by means of Veinoplusยฎ 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.

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 Owner
Short Name
Ad Rem Technology
Address
162, rue du Faubourg Saint Honore, 75008 Paris, FRANCE
Registrant
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