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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 IMP/MD/2023/000244_d69bc356951cb011ba7eb177911663b8_2ddd74cce8c31792dec66d4855d64e25. The license holder is KARL STORZ ENDOSCOPY INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Guide Wire
UID: IMP/MD/2023/000244_d69bc356951cb011ba7eb177911663b8_2ddd74cce8c31792dec66d4855d64e25

Device Class

Class B

Approving Authority

CDSCO

Product Information

Guide wires are used for ensuring the precise insertion of cannulated instruments/implants in arthroscopy and in minimally invasive orthopedics. Guide wires are designed for transient use in surgically invasive interventions. Dilators/bougies are used to expand tissue to create an access tract to the punctured organ ##PLACEHOLDER_0## up to the diameter necessary for the intervention. The dilator/bougie is inserted via a guide wire which is advanced through a puncture cannula. The sheath is then positioned via the dilator/bougie in the renal collecting system/bladder. The dilator/bougie is designed for transient use in surgically invasive interventions

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