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Hydrophilic Guide Wire - India CDSCO Medical Device Registration

Hydrophilic Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000049_7e9b58b5ec26ae599e330fcb95f9fab7_b030fd7f2e32f7fd4868abbb00a6cad1. This device is marketed under the brand name Carry. The license holder is Dr. Surgical, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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 D
Hydrophilic Guide Wire
UID: MFG/MD/2019/000049_7e9b58b5ec26ae599e330fcb95f9fab7_b030fd7f2e32f7fd4868abbb00a6cad1

Brand Name

Carry

License Holder

Dr. Surgical

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Guidewire facilitates placement of a catheter during diagnostic or interventional peripheral intravascular procedures including but not limited to renal intervention. The wire can be torqued to facilitate navigation through the vasculature. All Hi-Torque Guide Wires are intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (Carry) and percutaneous transluminal angioplasty (Carry)

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