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Respiratory PAP - India CDSCO Medical Device Registration

Respiratory PAP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000757_3b0d4a2aecd1700e4d709cdfc2ef5ce2_5e6bb82ead7604deaf2e43f25a5bc59e. This device is marketed under the brand name BPL. The license holder is BPL MEDICAL TECHNOLOGIES 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
Respiratory PAP
UID: IMP/MD/2023/000757_3b0d4a2aecd1700e4d709cdfc2ef5ce2_5e6bb82ead7604deaf2e43f25a5bc59e

Brand Name

BPL

Device Class

Class B

Approving Authority

CDSCO

Product Information

The BPL LIFEPAP SERIES delivers positive airway pressure therapy for the treatment of Obstructive Sleep Apnea (BPL) in spontaneously breathing patients weighting over 30kg (BPL) and can be used at home, hospital, or institutional environment. The system is also intended for spot check transcutaneous measurement of oxygen saturation (BPL) in the blood using light detection given from a special probe for adults and pediatrics. This spot check transcutaneous measurement of oxygen saturation (BPL) is an optional feature

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