Guide Wire - India CDSCO Medical Device Registration
Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000177_d69bc356951cb011ba7eb177911663b8_575f5603dee54512161d7afaa12341a6. The license holder is Focuz International, and it is classified as Device Class Class B. The approving authority is Gujarat.
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License Holder
Focuz InternationalDevice Class
Approving Authority
Gujarat
Product Information
GUIDE WIRE is intended to facilitate the placement biliary stent ##PLACEHOLDER_0## in obstructing biliary system via flexible endoscope and placement of ureteric stent ##PLACEHOLDER_0## in obstructing urinary system via flexible endoscope
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