MANIFOLD
- UID
- MFG/MD/2020/000113_9dbaa6e6cafc0d78c8d831d11106f356_18f6e3017bb5b8bb818ae700c8dc6ba6
- Device class
- Class B
- Brand name
- SURETECH
- License holder
- Suretech Medical Inc
- Approving authority
- Greater Mumbai Division
- Product information
- INDICATED FOR FLUID FLOW DIRECTION CONTROL AND PROVIDING ACCESS PORT/PORTS FOR ADMINISTRATION OF A SOLUTION
MANIFOLD is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000113_9dbaa6e6cafc0d78c8d831d11106f356_18f6e3017bb5b8bb818ae700c8dc6ba6. This device is marketed under the brand name SURETECH. The license holder is Suretech Medical Inc, and it is classified as Device Class Class B. The approving authority is Greater Mumbai Division.
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