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Single Use Resuscitator - India CDSCO Medical Device Registration

Single Use Resuscitator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000098_a2cf9babce20fa1994ba2e5407590d9b_14945e037c97dc149b71ae496846b018. This device is marketed under the brand name Flexicare. The license holder is FLEXICARE MEDICAL (INDIA) 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
Single Use Resuscitator
UID: IMP/MD/2019/000098_a2cf9babce20fa1994ba2e5407590d9b_14945e037c97dc149b71ae496846b018

Brand Name

Flexicare

Device Class

Class B

Approving Authority

CDSCO

Product Information

Flexicareโ€™s single use manual Resuscitator is intended for use on patients requiring artificial ventilation or ventilatory support in healthcare settings and emergency environments

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