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ACE Test Kit - India CDSCO Medical Device Registration

ACE Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_9803eef68ac2dee1fa51cb0ad26efc0f_8a4d99fb5270c0aff10b336399ca08e9. This device is marketed under the brand name 1:1. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class B. 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 B
ACE Test Kit
UID: MFG/IVD/2022/000015_9803eef68ac2dee1fa51cb0ad26efc0f_8a4d99fb5270c0aff10b336399ca08e9

Brand Name

1:1

Device Class

Class B

Approving Authority

Kokan Division

Product Information

For in vitro quantitative determination of angiotensin converting enzyme activity in serum

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