CDSCO UID MFG/MD/2023/000026_9e5123f2acfbb3f091d2e22562fd9866_0681550098a456b3c2c293e5238883b5

Highly cross-linked sodium hyaluronate 23 mg/ ml with 0.3% lidocaine hydrochloride

REENAV LOGISTICS PVT LTD·Device Class Class C·India CDSCO·Brand: Secondary Packing / Labeling / Stickering / Overprinting / Stamping
Registration details
UID
MFG/MD/2023/000026_9e5123f2acfbb3f091d2e22562fd9866_0681550098a456b3c2c293e5238883b5
Device class
Class C
Brand name
Secondary Packing / Labeling / Stickering / Overprinting / Stamping
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
The device is indicated to correct moderate to severe nasolabial folds. It is indicated to be injected into the deep dermis or subcutis. The intended purpose of the device is to create volume in order to correct wrinkles and folds, and to correct moderate to severe nasolabial folds to treat signs of ageing
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Products from the same license holder (4 products)
Monofilament Synthetic Absorbable Skin Support and Filling Thread Sterile
Brand: Secondary Packing / Labeling / Stickering / Overprinting / Stamping
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Monofilament Synthetic Absorbable Skin Support and Filling Thread Sterile
Brand: Secondary Packing / Labeling / Stickering / Overprinting / Stamping
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Cross-linked sodium hyaluronate 23 mg/ml with 0.3% lidocaine hydrochloride
Brand: Secondary Packing / Labeling / Stickering / Overprinting / Stamping
Class C
Cross-linked sodium hyaluronate 25 mg/mL with 0.3% lidocaine hydrochloride
Brand: Secondary Packing / Labeling / Stickering / Overprinting / Stamping
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About this record

Highly cross-linked sodium hyaluronate 23 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_9e5123f2acfbb3f091d2e22562fd9866_0681550098a456b3c2c293e5238883b5. 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 C. The approving authority is Central Drug Standards Control Organization, West Zone.

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