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RETIJET® - India CDSCO Medical Device Registration

RETIJET® is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000414_fc8ebc712610a3225b48b3f26cc99585_3be2308569af7ffb2f308dcf8bcd53b0. This device is marketed under the brand name CONFORMER. The license holder is Carl Zeiss India (Bangalore) 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
RETIJET®
UID: IMP/MD/2019/000414_fc8ebc712610a3225b48b3f26cc99585_3be2308569af7ffb2f308dcf8bcd53b0

Brand Name

CONFORMER

Device Class

Class B

Approving Authority

CDSCO

Product Information

RETIJET® is designed to enable either injection of FCI PURIFIED SILICONE OIL SYRINGE or extraction of silicone oil through a trocar placed in the pars plana before the extraction

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