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FUSION™ Pack - India CDSCO Medical Device Registration

FUSION™ Pack is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000222_32f92d066c9d4d0ec3a6bd8a1e47c449_78f6516060764acfc37bb877b44a5721. This device is marketed under the brand name 23 Gauge Vitrectomy Cutter. 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
FUSION™ Pack
UID: IMP/MD/2023/000222_32f92d066c9d4d0ec3a6bd8a1e47c449_78f6516060764acfc37bb877b44a5721

Brand Name

23 Gauge Vitrectomy Cutter

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FUSION™ DUAL PUMP Pack is used with the WHITESTAR SIGNATURE™ system. The FUSIONTM DUAL PUMP Pack is sterilized by irradiation and is designed for single use only

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