Cross-linked sodium hyaluronate 25 mg/mL with 0.3% lidocaine hydrochloride
- UID
- MFG/MD/2023/000026_18926b2de5d2ce5a49d93fc353abf183_44cfab7c41f570914b8985637e79b0e0
- Device class
- Class D
- Brand name
- Secondary Packing / Labeling / Stickering / Overprinting / Stamping
- License holder
- REENAV LOGISTICS PVT LTD
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- The device is indicated to correct moderate to severe midface volume deficit in the zygomaticomalar region, anteromedial cheek region and submalar region. The device has to be administered by deep subcuteaneous and/or supraperiosteal injection. The intended purpose of the device is to restore facial volume in order to correct moderate to severe midface volume deficit to treat signs of ageing.
Cross-linked sodium hyaluronate 25 mg/mL with 0.3% lidocaine hydrochloride is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000026_18926b2de5d2ce5a49d93fc353abf183_44cfab7c41f570914b8985637e79b0e0. This device is marketed under the brand name Secondary Packing / Labeling / Stickering / Overprinting / Stamping. The license holder is REENAV LOGISTICS PVT LTD, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.
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