Annuloplasty Device - India CDSCO Medical Device Registration
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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Brand Name
Memo 3D ReChord Semirigid Annuloplasty Ring
License Holder
LIVANOVA INDIA PVT. LTD.Device Class
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
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Parekh Integrated Services Pvt. Ltd.
Annuloplasty Device
Brand: Sovering Annuloplasty Device
Parekh Integrated Services Pvt. Ltd.
Annuloplasty Device
Brand: Sovering Annuloplasty Device
Parekh Integrated Services Pvt. Ltd.
Annuloplasty Device
Brand: Sovering Annuloplasty Device
Parekh Integrated Services Pvt. Ltd.
Annuloplasty Device
Brand: Memo 3D ReChord Semirigid Annuloplasty Ring
LIVANOVA INDIA PVT. LTD.
Annuloplasty Device
Brand: Memo 3D ReChord Semirigid Annuloplasty Ring
LIVANOVA INDIA PVT. LTD.
Annuloplasty Device
Brand: Memo 3D ReChord Semirigid Annuloplasty Ring
LIVANOVA INDIA PVT. LTD.
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