Copper Test Kit - India CDSCO Medical Device Registration
Copper Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_cecb66e1ca6b95699098d3b74ce1f30e_c7cdb6348961fa25b6db9780d13eab57. 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.
Brand Name
1:1
License Holder
DiaSys Diagnostics India Private LimitedDevice Class
Approving Authority
Kokan Division
Product Information
Diagnostic reagent for in vitro quantitative determination of copper in human serum on photometric analyzers
Gamma GT Reagent Test kit
Brand: 1:1
DiaSys Diagnostics India Private Limited
Creatinine Reagent test kit
Brand: 1:1
DiaSys Diagnostics India Private Limited
QDx InstaLyte Universal Disposable
Brand: 1:1
DiaSys Diagnostics India Private Limited
ISE standard for biochemistry analyzer
Brand: 1:1
DiaSys Diagnostics India Private Limited
ACE Test Kit
Brand: 1:1
DiaSys Diagnostics India Private Limited
ADA Control
Brand: 1:1
DiaSys Diagnostics India Private Limited
ADA Test Kit
Brand: 1:1
DiaSys Diagnostics India Private Limited
ADA Test Kit
Brand: 1:1
DiaSys Diagnostics India Private Limited

