CDSCO UID MFG/MD/2023/000313_7cb407104cb2d917e2c129a8bf681b78_0d26e2c59fd9ae9a4d51520f4de13316

Spirometer

NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.·Device Class Class B·India CDSCO·Brand: ReMeDi

Registration details

UID: MFG/MD/2023/000313_7cb407104cb2d917e2c129a8bf681b78_0d26e2c59fd9ae9a4d51520f4de13316
Device class: Class B
Brand name: ReMeDi
License holder: NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.
Approving authority: Karnataka
Product information: ReMeDi® 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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About this record

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.

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