Artificial lung ventilation apparatus with controlled modes of operation in terms of volume, pressure and auxiliary automatic self-testing and an alarm system for violations of operating modes for adults and children over one year old ELAN-R
- Device Name (English)
- Artificial lung ventilation apparatus with controlled modes of operation in terms of volume, pressure and auxiliary automatic self-testing and an alarm system for violations of operating modes for adults and children over one year old ELAN-R
- Device Name (Russian)
- Аппарат искусственной вентиляции легких с управляемыми режимами работы по объему давлению и вспомогательным автоматическим самотестированием и системой сигнализации при нарушениях режимов работы для взрослых и детей старше одного года ЭЛАН-Р
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o27899
- Registration Number
- ФС 022а2005/2514-05
- Registration Date
- December 01, 2005
- Validity Period
- December 01, 2010
- Manufacturer Name (English)
- JSC VNIIMP-VITA
- Manufacturer Name (Russian)
- ЗАО ВНИИМП-ВИТА
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Moscow
- Legal Address (Russian)
- Москва
Access comprehensive regulatory information for Artificial lung ventilation apparatus with controlled modes of operation in terms of volume, pressure and auxiliary automatic self-testing and an alarm system for violations of operating modes for adults and children over one year old ELAN-R in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФС 022а2005/2514-05 and manufactured by JSC VNIIMP-VITA. The device was registered on December 01, 2005.
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.