X-ray devices of the BV series of versions without sources of radioactive radiation (see Appendix on 3 sheets) The series of X-ray devices BV (without sources of radioactive radiation) includes the following versions: - BV Pulsera - mobile X-ray machine - BV Endura - mobile ... (see the full description in the card)
- Device Name (English)
- X-ray devices of the BV series of versions without sources of radioactive radiation (see Appendix on 3 sheets) The series of X-ray devices BV (without sources of radioactive radiation) includes the following versions: - BV Pulsera - mobile X-ray machine - BV Endura - mobile ... (see the full description in the card)
- Device Name (Russian)
- Аппараты рентгеновские серии BV версий без источников радиоактивного излучения (см.Приложение на 3-х листах) Серия аппаратов рентгеновских BV (без источников радиоактивного излучения) включает нижепоименованные версии: - BV Pulsera - передвижной рентгеновский аппарат - BV Endura - передвижной ... (см. в карточке полное описание)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o63691
- Registration Number
- МЗ РФ № 2003/342
- Registration Date
- March 17, 2003
- Validity Period
- March 17, 2013
- Manufacturer Name (English)
- Phillips Medical Systems
- Manufacturer Name (Russian)
- Филипс Медицинские Системы
- Country (English)
- GERMANY
- Country (Russian)
- ФРГ
- Legal Address (English)
- GERMANY
- Legal Address (Russian)
- ФРГ
Access comprehensive regulatory information for X-ray devices of the BV series of versions without sources of radioactive radiation (see Appendix on 3 sheets) The series of X-ray devices BV (without sources of radioactive radiation) includes the following versions: - BV Pulsera - mobile X-ray machine - BV Endura - mobile ... (see the full description in the card) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2003/342 and manufactured by Phillips Medical Systems. The device was registered on March 17, 2003.
This page provides complete registration details including device type, manufacturer information, country of origin (GERMANY), 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.