Percutaneous Transluminal Angioplasty Catheter
- UID
- IMP/MD/2019/000511_159f1c310eed0f0711fd8c25ce58c4fc_dc6e97fdb96b02b1537ad2e54c98879a
- Device class
- Class B
- Brand name
- PTA
- License holder
- Abbott Healthcare Private Limited
- 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
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.
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