Percutaneous Transluminal Angioplasty Catheter - India CDSCO Medical Device Registration

Percutaneous Transluminal Angioplasty Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000511_159f1c310eed0f0711fd8c25ce58c4fc_dc6e97fdb96b02b1537ad2e54c98879a. This device is marketed under the brand name PTA. The license holder is Abbott Healthcare Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database

CDSCO Registered

Class Class B

Percutaneous Transluminal Angioplasty Catheter

UID: IMP/MD/2019/000511_159f1c310eed0f0711fd8c25ce58c4fc_dc6e97fdb96b02b1537ad2e54c98879a

Brand Name

PTA

License Holder

Abbott Healthcare Private Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Armada 18 is indicated to dilate stenosis in femoral, popliteal, infra-popliteal, tibial, peroneal, and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. In addition, the device is also indicated for post-dilatation of balloon expandable and self-expanding stents