Annuloplasty Device
- UID
- IMP/MD/2018/000392_2f94374abd14ee777b52bfec9c00c5c3_521ce3e4d3710755a09febdb9df05e63
- Device class
- Class C
- Brand name
- Memo 3D ReChord Semirigid Annuloplasty Ring
- License holder
- LIVANOVA INDIA PVT. LTD.
- Approving authority
- CDSCO
- Product information
- It is indicated as reinforcement for repair of the human cardiac tricuspid valve damaged by acquired or congenital disease, or as a replacement for a previously implanted Annuloplasty ring
Annuloplasty Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000392_2f94374abd14ee777b52bfec9c00c5c3_521ce3e4d3710755a09febdb9df05e63. This device is marketed under the brand name Memo 3D ReChord Semirigid Annuloplasty Ring. The license holder is LIVANOVA INDIA PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.
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