Control materials for the hematological analyzer ADVIA 120 (see Appendix on sheet 1) 1. ADVIA 120 Testpoint 3 in 1 Normal ADVIA 120 3 in 1 TESTpoint Normal packing: 4 x 4 ml 3. ADVIA 120 Testpoint 3 in 1 Abnormal 2 ADVIA 120 3 in 1 TESTpoint Abnormal 2 Packing: 4 x 4 ml 2. ADVIA 120 Testpoint 3 in 1 Abnormal 1 ADVIA 120 3 in 1 TESTpoint Abnormal 1 pack: 4 x 4 ml - Roszdravnadzor Registration МЗ РФ № 2004/215

Access comprehensive regulatory information for Control materials for the hematological analyzer ADVIA 120 (see Appendix on sheet 1) 1. ADVIA 120 Testpoint 3 in 1 Normal ADVIA 120 3 in 1 TESTpoint Normal packing: 4 x 4 ml 3. ADVIA 120 Testpoint 3 in 1 Abnormal 2 ADVIA 120 3 in 1 TESTpoint Abnormal 2 Packing: 4 x 4 ml 2. ADVIA 120 Testpoint 3 in 1 Abnormal 1 ADVIA 120 3 in 1 TESTpoint Abnormal 1 pack: 4 x 4 ml in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2004/215 and manufactured by Bayer Corporation. The device was registered on March 05, 2004.

This page provides complete registration details including device type, manufacturer information, country of origin (USA), and regulatory compliance data from the official Russia Roszdravnadzor medical device database. Pure Global AI offers free access to Russia's complete medical device registry, helping global MedTech companies navigate Roszdravnadzor regulations efficiently.