GUIDEWIRE - India CDSCO Medical Device Registration
GUIDEWIRE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000041_5a35ad56ad19332e653127505267b213_9e1a15a5c948f9b36cd9fc9c1cfc975b. The license holder is Blue Neem Medical Devices Private Limited, and it is classified as Device Class Class B. The approving authority is Karnataka.
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License Holder
Blue Neem Medical Devices Private LimitedDevice Class
Approving Authority
Karnataka
Product Information
Used primarily to establish a tract and assist in the placement of a surgical device during urology procedures
