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Vyntus® APS - India CDSCO Medical Device Registration

Vyntus® APS is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000638_10fd4b9b373f91dabda97697be1ddbf3_ff0d5532cc88b56d0b226dbc5e9086bc. This device is marketed under the brand name Vyaire™ Medical. The license holder is Genworks Health Private Limited, 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.

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CDSCO Registered
Class Class B
Vyntus® APS
UID: IMP/MD/2023/000638_10fd4b9b373f91dabda97697be1ddbf3_ff0d5532cc88b56d0b226dbc5e9086bc

Brand Name

Vyaire™ Medical

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Vyntus APS consists of the extended basic module with an integrated compressor and a nebulizer unit. In combination with the Vyntus PNEUMO and/or the Vyntus IOS, the Vyntus APS is used to observe the provocation test. The software-controlled Vyntus APS (Vyaire™ Medical) allows easy and reproducible administration of different aerosols for specific and non-specific provocation tests in order to examine the reaction of a patient's respiratory system to the administered aerosols

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