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PTCA Guidewire - India CDSCO Medical Device Registration

PTCA Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000341_4167d2d482cf70301fd4d8aec499ad2d_700b0b2bab480629eff88ee87dd99ce0. This device is marketed under the brand name ACE. The license holder is Biorad Medisys Pvt Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West 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 D
PTCA Guidewire
UID: MFG/MD/2022/000341_4167d2d482cf70301fd4d8aec499ad2d_700b0b2bab480629eff88ee87dd99ce0

Brand Name

ACE

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Intended for interventional cardiology procedures

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