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VitriFit - India CDSCO Medical Device Registration

VitriFit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000219_d0283f46b3c8084a6a29e4a84304a9c5_aec54387ff49d839d931aa57e39807ff. This device is marketed under the brand name VitriFit. The license holder is Origio 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
VitriFit
UID: IMP/MD/2023/000219_d0283f46b3c8084a6a29e4a84304a9c5_aec54387ff49d839d931aa57e39807ff

Brand Name

VitriFit

Device Class

Class B

Approving Authority

CDSCO

Product Information

For storage of vitrified human oocytes, cleavage stage embryos and blastocysts.

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