3 Port Manifold Kit
- UID
- MFG/MD/2022/000130_84fd7f4784c3386e9c2e5ec1193aa1ca_55fc3982e5743f6fc44ffc7c5533da04
- Device class
- Class B
- Brand name
- Flexoline
- License holder
- George Philips Medical Engineering Pvt Ltd
- Approving authority
- Kokan Division
- Product information
- 3 Port Manifold Kits are intended to be used to establish connections between equipment’s and physiological monitoring equipment’s to monitor infusion and physiques
3 Port Manifold Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000130_84fd7f4784c3386e9c2e5ec1193aa1ca_55fc3982e5743f6fc44ffc7c5533da04. This device is marketed under the brand name Flexoline. The license holder is George Philips Medical Engineering Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.
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