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Phadia 200 - India CDSCO Medical Device Registration

Phadia 200 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000092_bf8f8cd775b6c9f6122d7483caffdd60_dd3c6dc595b0c9da02314f6cd74c7ee5. This device is marketed under the brand name NIL. The license holder is Thermo Fisher Scientific India Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Phadia 200
UID: IMP/IVD/2023/000092_bf8f8cd775b6c9f6122d7483caffdd60_dd3c6dc595b0c9da02314f6cd74c7ee5

Brand Name

NIL

Device Class

Class A

Approving Authority

CDSCO

Product Information

Phadia 200 is a fully automated instrument including software to be used together with dedicated in vitro diagnostic tests. The instrument is designed to handle processing of samples, reagents and calculation of analytical results from the measurement values. Phadia 200 is intended to be used in clinical laboratories.

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