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
- Device Name (English)
- 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
- Device Name (Russian)
- Материалы контрольные для гематологического анализатора ADVIA 120 (см. Приложение на 1 листе)1. АДВИЯ 120 Тестпоинт 3 в 1 Нормальный ADVIA 120 3 in 1 TESTpoint Normal упаковка: 4 x 4 мл 3. АДВИЯ 120 Тестпоинт 3 в 1 Абнормальный 2 ADVIA 120 3 in 1 TESTpoint Abnormal 2 упаковка: 4 x 4 мл 2. АДВИЯ 120 Тестпоинт 3 в 1 Абнормальный 1 ADVIA 120 3 in 1 TESTpoint Abnormal 1 упаковка: 4 x 4 мл
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o65520
- Registration Number
- МЗ РФ № 2004/215
- Registration Date
- March 05, 2004
- Validity Period
- March 05, 2009
- Manufacturer Name (English)
- Bayer Corporation
- Manufacturer Name (Russian)
- Bayer Corporation
- Country (English)
- USA
- Country (Russian)
- USA
- Legal Address (English)
- United States
- Legal Address (Russian)
- США
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.