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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/2021/000085_6f79c5dae2a086e749af43b13df8e910_36863a49b58fe33c7d38fc02f20dc4ae. This device is marketed under the brand name Shinewire. The license holder is M/s ST. STONE MEDICAL DEVICES PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is North East Sub Zone.

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 C
Guidewire
UID: MFG/MD/2021/000085_6f79c5dae2a086e749af43b13df8e910_36863a49b58fe33c7d38fc02f20dc4ae

Brand Name

Shinewire

Device Class

Class C

Approving Authority

North East Sub Zone

Product Information

It is intended to facilitate the placement of balloon of balloon dilation catheter during percutaneous transluminal coronary angioplasty (Shinewire) and percutaneous transluminal angioplasty(Shinewire)

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