Cordis SABER™ .035 Percutaneous Transluminal Angioplasty Catheter - HSA Registration DE0507902
Access comprehensive regulatory information for Cordis SABER™ .035 Percutaneous Transluminal Angioplasty Catheter in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0507902 and owned by Cordis Corporation. The device was registered on March 15, 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.
The SABER™ .035 PTA Balloon Dilatation catheter is intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also indicated for post-dilation of balloon-expandable and self-expanding stents in the peripheral vasculature.

