Pure Global

ASAHI Peripheral GuideWire - India CDSCO Medical Device Registration

ASAHI Peripheral GuideWire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000492_0bca2e9f028b63a16fcf09162046bae8_ce1df3a0f7ce54734e596da93a297015. This device is marketed under the brand name ASAHI Gladius MG & EX. The license holder is M/s. Asahi Intecc Co., Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.

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
Powered by Pure Global AI
CDSCO Registered
Class Class C
ASAHI Peripheral GuideWire
UID: IMP/MD/2019/000492_0bca2e9f028b63a16fcf09162046bae8_ce1df3a0f7ce54734e596da93a297015

Brand Name

ASAHI Gladius MG & EX

Device Class

Class C

Approving Authority

CDSCO

Product Information

This product is intended to facilitate the placement and exchange of diagnostic and therapeutic devices during intravascular procedures. This device is intended for peripheral vascular use only

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing