Pacemaker
- UID
- IMP/MD/2021/000379_d95adee972ae170512bd3bdbce557054_a750ab477d4c2f8f03d5fb05f7a2db79
- Device class
- Class D
- Brand name
- Cobalt™ XT DR MRI SureScan
- License holder
- India Medtronic Private Limited
- Approving authority
- CDSCO
- Product information
- Medtronic Relia Series implantable pulse generators (Cobalt™ XT DR MRI SureScan ) are indicated for use to improve cardiac output, prevent symptoms, or protect against arrhythmias related to cardiac impulse formation or conduction disorders. These devices are indicated for use in patients who are experiencing exercise intolerance or exercise restrictions related to an arrhythmia. Using rate response modes may restore heart rate variability and improve cardiac output. Relia SR Series implantable pulse generators are indicated for single use only
Pacemaker is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000379_d95adee972ae170512bd3bdbce557054_a750ab477d4c2f8f03d5fb05f7a2db79. This device is marketed under the brand name Cobalt™ XT DR MRI SureScan . The license holder is India Medtronic Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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