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REAGENT PACK FOR 931DT - India CDSCO Medical Device Registration

REAGENT PACK FOR 931DT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000330_86664ff572b9d139a0bc7e053d79123a_22668c9db182530d5a812e7c98ad88db. This device is marketed under the brand name CARETIUM. The license holder is LAB X, 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
REAGENT PACK FOR 931DT
UID: IMP/IVD/2021/000330_86664ff572b9d139a0bc7e053d79123a_22668c9db182530d5a812e7c98ad88db

Brand Name

CARETIUM

License Holder

LAB X

Device Class

Class B

Approving Authority

CDSCO

Product Information

For in vitro diagnostic use only , Use for only with XI-931 series electrolyte analyzers

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