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Angiotensin Converting Enzyme test Kit - India CDSCO Medical Device Registration

Angiotensin Converting Enzyme test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000117_cb09a3f8ad913d6c8d385bd17bf58890_f5cfa7a73529a9a854c9ede48e31e70d. This device is marketed under the brand name Cellpro. The license holder is Cellpro Systems Private Limited, and it is classified as Device Class Class B. The approving authority is Haryana.

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
Angiotensin Converting Enzyme test Kit
UID: MFG/IVD/2022/000117_cb09a3f8ad913d6c8d385bd17bf58890_f5cfa7a73529a9a854c9ede48e31e70d

Brand Name

Cellpro

Device Class

Class B

Approving Authority

Haryana

Product Information

The Angiotensin Converting Enzyme (Cellpro) Activity Assay is Detection of ACE1 activity in Tissue/Cell lysates, Serum, Plasma and Enables to screen for ACE inhibitors

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