Magnit-M-1000-"Med TeKo" magnetotherapy device according to TU 26.60.13-038-56812193-2019 Composed of: 1. Electronic unit - 1 pc. 2. Inductor No1 (solenoid) - 1 pc. 3. Inductor No2 (solenoid) - 1 pc. 4. Inductor No3 (waist) - 1 pc. 5. Operation manual - 1 pc.
- Device Name (English)
- Magnit-M-1000-"Med TeKo" magnetotherapy device according to TU 26.60.13-038-56812193-2019 Composed of: 1. Electronic unit - 1 pc. 2. Inductor No1 (solenoid) - 1 pc. 3. Inductor No2 (solenoid) - 1 pc. 4. Inductor No3 (waist) - 1 pc. 5. Operation manual - 1 pc.
- Device Name (Russian)
- Аппарат для магнитотерапии Магнит-М-1000-"Мед ТеКо" по ТУ 26.60.13-038-56812193-2019 в составе: 1. Электронный блок - 1 шт. 2. Индуктор №1 (соленоид) - 1 шт. 3. Индуктор №2 (соленоид) - 1 шт. 4. Индуктор №3 (поясной) - 1 шт. 5. Руководство по эксплуатации - 1 шт.
- Device Type (English)
- N/A
- Device Type (Russian)
- 285040
- Risk Class
- Class 2a
- OKPD Code
- 26.60.13.160
- Registry Key
- 75113.0
- Registration Number
- РЗН 2020/9780
- Registration Date
- December 14, 2023
- Manufacturer Name (English)
- ООО "Мед ТеКо"
- Manufacturer Name (Russian)
- ООО "Мед ТеКо"
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Med TeKo LLC, 16/2 Olimpiyskiy prospekt, Mytishchi, Moscow region, 141009, Russia
- Legal Address (Russian)
- ООО "Мед ТеКо", Россия, 141009, Московская область, г.о. Мытищи, г. Мытищи, Олимпийский пр-кт, д. 16, к. 2
- Manufacturing Address
- 141009, Россия, Московская область, г.о. Мытищи, г. Мытищи, Олимпийский пр-кт, д. 16, к. 2
Access comprehensive regulatory information for Magnit-M-1000-"Med TeKo" magnetotherapy device according to TU 26.60.13-038-56812193-2019 Composed of: 1. Electronic unit - 1 pc. 2. Inductor No1 (solenoid) - 1 pc. 3. Inductor No2 (solenoid) - 1 pc. 4. Inductor No3 (waist) - 1 pc. 5. Operation manual - 1 pc. in the Russia medical device market through Pure Global AI's free database. This Class 2a medical device is registered under Roszdravnadzor registration number РЗН 2020/9780 and manufactured by ООО "Мед ТеКо". The device was registered on December 14, 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.