Pure Global

Nasal Cannula - India CDSCO Medical Device Registration

Nasal Cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_05075d7566d11a61d28aabac1dc285be_434f3ee2ee1e0b86ddab074f6e16f51f. This device is marketed under the brand name Neopuff. The license holder is Fisher & Paykel Healthcare India Pvt Ltd ,3rd Floor, Unit Nos. 302-B & 303, Brigade Opus, No. 70/401, Kodigehalli Gate, Hebbal, Bangalore North Taluk, Bangalore-560092 ,Bengaluru (Bangalore) Urban Karnataka ,560092 ,India, and it is classified as Device Class Class B. 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 B
Nasal Cannula
UID: IMP/MD/2021/000505_05075d7566d11a61d28aabac1dc285be_434f3ee2ee1e0b86ddab074f6e16f51f

Brand Name

Neopuff

Device Class

Class B

Approving Authority

CDSCO

Product Information

A single use nasal cannula intended for use with a nasal high flow therapy system to deliver heated and humidified nasal high flow therapy to spontaneously breathing patients who require breathing support.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from Fisher & Paykel Healthcare India Pvt Ltd ,3rd Floor, Unit Nos. 302-B & 303, Brigade Opus, No. 70/401, Kodigehalli Gate, Hebbal, Bangalore North Taluk, Bangalore-560092 ,Bengaluru (Bangalore) Urban Karnataka ,560092 ,India
Products from the same license holder (8 products)