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Auto Hematology Analyzer - 3 Part - India CDSCO Medical Device Registration

Auto Hematology Analyzer - 3 Part is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000098_39bf01c957bd345098fca20327631c7b_4c5a8815bd1907680264f3bda197ac3d. This device is marketed under the brand name Mispa Uriskan 100 Plus. The license holder is Agappe Diagnostics Ltd, and it is classified as Device Class Class A. The approving authority is Kerala.

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
Auto Hematology Analyzer - 3 Part
UID: MFG/IVD/2022/000098_39bf01c957bd345098fca20327631c7b_4c5a8815bd1907680264f3bda197ac3d

Brand Name

Mispa Uriskan 100 Plus

Device Class

Class A

Approving Authority

Kerala

Product Information

Auto Hematology Analyzer is a quantitative Auto Hematology Analyzer and 3 part differential counter for in Vitro Diagnostic use in clinical laboratories. The purpose of this analyzer is to identify the normal patient, with all normal system-generated parameters, and to flag or identify patient results that require additional studies,3 Part Differential Hematology Analyzer(Mispa Uriskan 100 Plus)-This machine is intended for in vitro determination of complete blood count (Mispa Uriskan 100 Plus), Hemoglobin testing to deliver safe patient care

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