Reagent kit for immunoenzymatic determination of IgG antibodies to Toxoplasma gondii antigens in blood serum (plasma) "Toxoplasma IgG-ELISA", according to TU 21.20.23-1012-18619450-2023 Composed of: 1. Tablet - 1 pc. 2. Calibration samples - 5 x 1.5 ml. 3. Control serum - 1 x 1.5 ml. 4. Conjugate - 1 x 14 ml. 5. ELISA buffer - 1 x 50 ml. 6. Tetramethylbenzidine substrate solution (TM B) - 1 x 14 ml. 7. Washing solution concentrate - 1 x 22 ml. 8. Stop reagent - 1 x 14 ml. 9. Paper for gluing the tablet - 2 pcs. 10. Instructions for use - 1 pc. 11. Quality control passport (analytical passport) - 1 pc.
Russia·255760·HEMA LLC·Registered November 02, 2023·Class 2b- Device Name (English)
- Reagent kit for immunoenzymatic determination of IgG antibodies to Toxoplasma gondii antigens in blood serum (plasma) "Toxoplasma IgG-ELISA", according to TU 21.20.23-1012-18619450-2023 Composed of: 1. Tablet - 1 pc. 2. Calibration samples - 5 x 1.5 ml. 3. Control serum - 1 x 1.5 ml. 4. Conjugate - 1 x 14 ml. 5. ELISA buffer - 1 x 50 ml. 6. Tetramethylbenzidine substrate solution (TM B) - 1 x 14 ml. 7. Washing solution concentrate - 1 x 22 ml. 8. Stop reagent - 1 x 14 ml. 9. Paper for gluing the tablet - 2 pcs. 10. Instructions for use - 1 pc. 11. Quality control passport (analytical passport) - 1 pc.
- Device Name (Russian)
- Набор реагентов для имуноферментного определения IgG антител к антигенам Toxoplasma gondii в сыворотке (плазме) крови "Toxoplasma IgG-ИФА", по ТУ 21.20.23-1012-18619450-2023 в составе: 1. Планшет - 1 шт. 2. Калибровочные пробы - 5 х 1,5 мл. 3. Контрольная сыворотка - 1 х 1,5 мл. 4. Конъюгат - 1 х 14 мл. 5. ИФА-буфер - 1 х 50 мл. 6. Субстратный раствор тетраметилбензидина (ТМ Б) - 1 x 14 мл. 7. Концентрат отмывочного раствора - 1 х 22 мл. 8. Стоп-реагент - 1 x 14 мл. 9. Бумага для заклеивания планшета - 2 шт. 10. Инструкция по применению - 1 шт. 11. Паспорт контроля качества (аналитический паспорт) - 1 шт.
- Device Type (English)
- N/A
- Device Type (Russian)
- 255760
- Risk Class
- Class 2b
- OKPD Code
- 21.20.23.110
- Registry Key
- 73719.0
- Registration Number
- РЗН 2023/21473
- Registration Date
- November 02, 2023
- Manufacturer Name (English)
- HEMA LLC
- Manufacturer Name (Russian)
- ООО "ХЕМА"
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- LLC "KEMA", Russia, 143900, Moscow region, Balashikha, Trubetskaya str., vld. 2B
- Legal Address (Russian)
- ООО "ХЕМА", Россия, 143900, Московская область, г. Балашиха, ул. Трубецкая, влд. 2В
- Manufacturing Address
- 125319, Россия, Москва, ул. 4-я 8 марта, д. 3, к. 3, помещ. 2
Access comprehensive regulatory information for Reagent kit for immunoenzymatic determination of IgG antibodies to Toxoplasma gondii antigens in blood serum (plasma) "Toxoplasma IgG-ELISA", according to TU 21.20.23-1012-18619450-2023 Composed of: 1. Tablet - 1 pc. 2. Calibration samples - 5 x 1.5 ml. 3. Control serum - 1 x 1.5 ml. 4. Conjugate - 1 x 14 ml. 5. ELISA buffer - 1 x 50 ml. 6. Tetramethylbenzidine substrate solution (TM B) - 1 x 14 ml. 7. Washing solution concentrate - 1 x 22 ml. 8. Stop reagent - 1 x 14 ml. 9. Paper for gluing the tablet - 2 pcs. 10. Instructions for use - 1 pc. 11. Quality control passport (analytical passport) - 1 pc. in the Russia medical device market through Pure Global AI's free database. This Class 2b medical device is registered under Roszdravnadzor registration number РЗН 2023/21473 and manufactured by HEMA LLC. The device was registered on November 02, 2023.
This page provides complete registration details including device type, manufacturer information, country of origin (Russia), 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.