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RETIC TUBE - India CDSCO Medical Device Registration

RETIC TUBE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000007_f58ea0d01a9d72fc55c243c44ccab355_a0ba0e65f5fa1cb69139cc79184eb1d7. This device is marketed under the brand name UNIKON -480. The license holder is Vector Biotek Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is Gujarat.

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
RETIC TUBE
UID: MFG/IVD/2020/000007_f58ea0d01a9d72fc55c243c44ccab355_a0ba0e65f5fa1cb69139cc79184eb1d7

Brand Name

UNIKON -480

Device Class

Class A

Approving Authority

Gujarat

Product Information

for reticulocyte cell count determination of blood sample in haematology,3 PART DIFFERENTIAL CELL COUNTER FOR VETERNARY(UNIKON -480)-The Auto Haematology Analyzer is a quantitative, automatic haematology 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. For the quantitative determination of RBC, WBC and Platelets

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