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Body Plethysmography - India CDSCO Medical Device Registration

Body Plethysmography is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000834_c12b10b00b2b4599bb26e6baebbb0fb7_7b28066efb27793b49a5a5d6034cac4d. This device is marketed under the brand name PowerCube + Series. The license holder is Schiller Healthcare India Pvt Ltd, 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
Body Plethysmography
UID: IMP/MD/2023/000834_c12b10b00b2b4599bb26e6baebbb0fb7_7b28066efb27793b49a5a5d6034cac4d

Brand Name

PowerCube + Series

Device Class

Class B

Approving Authority

CDSCO

Product Information

The PowerCube Series is intended to be used for measurement, data collection and analysis of lung function (Pulmonary function testing (PowerCube + Series)) parameters, aiding the healthcare provider in the diagnosis of respiratory related conditions. The testing can be performed on patients over 5 years old, in general practice, industrial, hospital and university settings, and by specialty physicians

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