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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 MFG/MD/2022/000092_3b0d4a2aecd1700e4d709cdfc2ef5ce2_30cc11c087456a54ca87d2507f5099e0. This device is marketed under the brand name BPL. The license holder is BPL Medical Technologies Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kerala.

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: MFG/MD/2022/000092_3b0d4a2aecd1700e4d709cdfc2ef5ce2_30cc11c087456a54ca87d2507f5099e0

Brand Name

BPL

Device Class

Class B

Approving Authority

Kerala

Product Information

It is indicated for treatment of sleep apnea hypopnea syndrome in patients weighing more than 66lb (BPL). It is intended both for home use and hospital use. The intended usage is to provide air flow of suitable temperature and humidity, which could effectively avoid the dryness of the nasopharyngeal mucosa in patients, and improve the comfort of patients during treatment

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