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Guide Wire - India CDSCO Medical Device Registration

Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000272_d42dbdb38e9d071dcab84df3c925fabd_cdcca672a5222038d0989c5acbd15ddd. This device is marketed under the brand name 240 Specifications. The license holder is MEDTECH DEVICES, 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
Guide Wire
UID: MFG/MD/2020/000272_d42dbdb38e9d071dcab84df3c925fabd_cdcca672a5222038d0989c5acbd15ddd

Brand Name

240 Specifications

License Holder

MEDTECH DEVICES

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Guidewire is used to guide catheter to lesion artery in angiography procedure

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