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/2019/000201_6f79c5dae2a086e749af43b13df8e910_602b373b7007f19142c3717a9c77dc71. This device is marketed under the brand name ClearSheath. The license holder is Newtech Medical Devices, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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.

Free Database

CDSCO Registered

Class Class C

Guidewire

UID: MFG/MD/2019/000201_6f79c5dae2a086e749af43b13df8e910_602b373b7007f19142c3717a9c77dc71

Brand Name

ClearSheath

License Holder

Newtech Medical Devices

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

It delivers radio opaque media and therapeutic agents to selected sites in the vascular system. It is also used to lead a guide wire or a catheter into the target site.