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Spirometer - India CDSCO Medical Device Registration

Spirometer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000313_7cb407104cb2d917e2c129a8bf681b78_0d26e2c59fd9ae9a4d51520f4de13316. This device is marketed under the brand name ReMeDi. The license holder is NEUROSYNAPTIC COMMUNICATIONS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Karnataka.

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
Spirometer
UID: MFG/MD/2023/000313_7cb407104cb2d917e2c129a8bf681b78_0d26e2c59fd9ae9a4d51520f4de13316

Brand Name

ReMeDi

Device Class

Class B

Approving Authority

Karnataka

Product Information

ReMeDiยฎ Spirometer is to be used only for spot check or non-invasive diagnostic functioning of lungs by measuring the volume of air inspired or expired by the lungs through wireless mode in home / healthcare facility environment

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