CDSCO UID MFG/MD/2020/000012_f95248b80b7bdad7c7c6d4cfc24c3be2_b43ccd168cec0a7c9e194b8e5282666cCoronary Artery Bypass Graft
- UID
- MFG/MD/2020/000012_f95248b80b7bdad7c7c6d4cfc24c3be2_b43ccd168cec0a7c9e194b8e5282666c
- Device class
- Class D
- Brand name
- PROLENE*
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Surgical Procedures relared to Coronary Artery Bypass
Coronary Artery Bypass Graft is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000012_f95248b80b7bdad7c7c6d4cfc24c3be2_b43ccd168cec0a7c9e194b8e5282666c. This device is marketed under the brand name PROLENE*. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.
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