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HiCrome™ Staph Agar Plate, Modified - India CDSCO Medical Device Registration

HiCrome™ Staph Agar Plate, Modified is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000105_f60025bfb98e804375a0843dcbbeb2e8_b261395eed011187aef44d6b7dfdd4de. This device is marketed under the brand name HiMedia. The license holder is HiMedia Laboratories Pvt Ltd., and it is classified as Device Class Class A. The approving authority is Kokan Division.

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
HiCrome™ Staph Agar Plate, Modified
UID: MFG/IVD/2023/000105_f60025bfb98e804375a0843dcbbeb2e8_b261395eed011187aef44d6b7dfdd4de

Brand Name

HiMedia

Device Class

Class A

Approving Authority

Kokan Division

Product Information

"HiCrome™ Staph Agar Plate, Modified selective medium for the isolation and enumeration of Staphylococcus aureus."

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