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I/A Handpiece - India CDSCO Medical Device Registration

I/A Handpiece is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000394_04941328896f43deda9ce0a9e64485a4_578f31798f419ad2c31594a5dcf9b9c9. This device is marketed under the brand name PHACOFIT® Titanium Handle. The license holder is Johnson & Johnson Surgical Vision India Pvt Ltd, 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
I/A Handpiece
UID: IMP/MD/2023/000394_04941328896f43deda9ce0a9e64485a4_578f31798f419ad2c31594a5dcf9b9c9

Brand Name

PHACOFIT® Titanium Handle

Device Class

Class B

Approving Authority

CDSCO

Product Information

The PHACOFIT® Titanium I/A Handpiece and Tips are indicated for use during cataract extraction to provide irrigation and aspiration functions. They havebeen designed for use with the AMO families of Phacoemulsification machines.

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