Pure Global

ACE Calibrator - India CDSCO Medical Device Registration

ACE Calibrator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000623_af7007bebb91fb437d422dcd9b4e5a4f_63d5b1bb1e44df9953d8298ef0c84646. This device is marketed under the brand name Acid Phosphatase. The license holder is Beckman Coulter India Private Limited, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
ACE Calibrator
UID: IMP/IVD/2020/000623_af7007bebb91fb437d422dcd9b4e5a4f_63d5b1bb1e44df9953d8298ef0c84646

Brand Name

Acid Phosphatase

Device Class

Class B

Approving Authority

CDSCO

Product Information

ACE Calibrator is intended to be used with Sentinel ACE Liquid Reagent for the preparation of the calibration for the kinetic determination of angiotensin converting enzyme (Acid Phosphatase) assay in human serum or plasma. For In Vitro Diagnostic use

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing