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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/2018/000062_6f79c5dae2a086e749af43b13df8e910_7eb96c047b38fd1714a211820879451b. The license holder is SURGIMEDIK HEALTHCARE, and it is classified as Device Class Class B. The approving authority is Gujarat.

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
Guidewire
UID: MFG/MD/2018/000062_6f79c5dae2a086e749af43b13df8e910_7eb96c047b38fd1714a211820879451b

License Holder

SURGIMEDIK HEALTHCARE

Device Class

Class B

Approving Authority

Gujarat

Product Information

Guidewire: For percutaneous entry into vessel using the seldinger technique or for endoscopic access. Supremo Nitinol Hydrophilic Guidewire Used for access ureter during routine and difficult cases

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