Ultrasonic inhaler OMRON NE U-22 (NE-U22-E) consisting of (see Appendix on 1 sheet) 1. Main appliance cover 2. Main device 3. Container for the drug 4. Spray head with membrane 5. Mask adapter 6. Mouthpiece 7. Small mask 8. Mask standard 9. Storage Case 10. Batteries 11. Instruction
Russia·Unknown·OMRON Matsusaka Co. Ltd.·Registered December 15, 2003·N/A- Device Name (English)
- Ultrasonic inhaler OMRON NE U-22 (NE-U22-E) consisting of (see Appendix on 1 sheet) 1. Main appliance cover 2. Main device 3. Container for the drug 4. Spray head with membrane 5. Mask adapter 6. Mouthpiece 7. Small mask 8. Mask standard 9. Storage Case 10. Batteries 11. Instruction
- Device Name (Russian)
- Ингалятор ультразвуковой OMRON NE U-22 (NE-U22-E) в составе (см. Приложение на 1 листе)1. Крышка основного прибора 2. Основной прибор 3. Контейнер для лекарственного препарата 4. Распылительная головка с мембраной 5. Переходник маски 6. Загубник 7. Маска малая 8. Маска стандартная 9. Чехол для хранения 10. Элементы питания 11. Инструкция
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o65034
- Registration Number
- МЗ РФ № 2003/1563
- Registration Date
- December 15, 2003
- Validity Period
- December 15, 2013
- Manufacturer Name (English)
- OMRON Matsusaka Co. Ltd.
- Manufacturer Name (Russian)
- OMRON Matsusaka Co. Ltd.
- Country (English)
- Japan
- Country (Russian)
- Japan
- Legal Address (English)
- Japan
- Legal Address (Russian)
- Япония
Access comprehensive regulatory information for Ultrasonic inhaler OMRON NE U-22 (NE-U22-E) consisting of (see Appendix on 1 sheet) 1. Main appliance cover 2. Main device 3. Container for the drug 4. Spray head with membrane 5. Mask adapter 6. Mouthpiece 7. Small mask 8. Mask standard 9. Storage Case 10. Batteries 11. Instruction in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2003/1563 and manufactured by OMRON Matsusaka Co. Ltd.. The device was registered on December 15, 2003.
This page provides complete registration details including device type, manufacturer information, country of origin (Japan), 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.