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Muller Hinton E Agar - India CDSCO Medical Device Registration

Muller Hinton E Agar is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000818_ee1e9db2b7bffeeb8f37f85983bd0157_947acb3024df19e8abe6ed455bacfd70. This device is marketed under the brand name chromIDโ„ข VRE Agar. The license holder is BioMerieux 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
Muller Hinton E Agar
UID: IMP/IVD/2020/000818_ee1e9db2b7bffeeb8f37f85983bd0157_947acb3024df19e8abe6ed455bacfd70

Brand Name

chromIDโ„ข VRE Agar

Device Class

Class B

Approving Authority

CDSCO

Product Information

Study of antimicrobial susceptibility

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