CDSCO UID MFG/MD/2022/000509_95373924478f334ce26c72cd209efd16_641037963058c85d113fb6c7df113fbd
Monofilament Polypropylene Mesh
TTG INNOVATIONS PRIVATE LIMITED, C/O M/s SUGII SURGICAL INDIA PVT. LTD.·Device Class Class C·India CDSCO·Brand: STERGIC
Registration details
- UID
- MFG/MD/2022/000509_95373924478f334ce26c72cd209efd16_641037963058c85d113fb6c7df113fbd
- Device class
- Class C
- Brand name
- STERGIC
- Approving authority
- Sub Zonal Bangalore
- Product information
- MONOFILAMENT POLYPROPYLENE MESH is used for abdominal wall reinforcement, treatment of incisional, inguinal, femoral, umbilical and ventral hernias. It is used in both colposcopy and laparotomy. It is used for the repair of hernia, utero-vaginal prolapse and other facial deficiencies that require the addition of a reinforcing or bridging material to obtain the desired surgical result
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About this record
Monofilament Polypropylene Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000509_95373924478f334ce26c72cd209efd16_641037963058c85d113fb6c7df113fbd. This device is marketed under the brand name STERGIC. The license holder is TTG INNOVATIONS PRIVATE LIMITED, C/O M/s SUGII SURGICAL INDIA PVT. LTD., and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.
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