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Silicone Anaesthetic Face Mask - India CDSCO Medical Device Registration

Silicone Anaesthetic Face Mask is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000098_e85e5906694e16fce0af9500536a99d0_c94ec091259d2cf716d0189f8da68e91. This device is marketed under the brand name ProVu. 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
Silicone Anaesthetic Face Mask
UID: IMP/MD/2019/000098_e85e5906694e16fce0af9500536a99d0_c94ec091259d2cf716d0189f8da68e91

Brand Name

ProVu

Device Class

Class B

Approving Authority

CDSCO

Product Information

Flexicareโ€™s Silicone Reusable Anaesthesia Face Masks are designed to channel anaesthesia gases or mixtures of oxygen to the patient for inhalation via the mouth and nose. Anaesthesia masks are to be used in conjunction with anaesthesia and ventilator breathing systems. They are reusable and fully autoclavable up to 50 times. The moulded texture of the rim ensures maximum patient comfort and a tight seal, while the transparent face piece allows patient monitoring at all times

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