Devices for measuring blood pressure and pulse rate digital automatic models BD 8500 BD 8700 with accessories (see Appendix on sheet 1)Equipment BD 8500: 1. Electronic unit 2. Cuff 3. Box for the device Equipment BD 8700: 1. Electronic unit 2. Cuff with rubber tube 3. Power supply for mains operation 4. Box for the appliance
- Device Name (English)
- Devices for measuring blood pressure and pulse rate digital automatic models BD 8500 BD 8700 with accessories (see Appendix on sheet 1)Equipment BD 8500: 1. Electronic unit 2. Cuff 3. Box for the device Equipment BD 8700: 1. Electronic unit 2. Cuff with rubber tube 3. Power supply for mains operation 4. Box for the appliance
- Device Name (Russian)
- Приборы для измерения артериального давления и частоты пульса цифровые автоматические моделей BD 8500 BD 8700 с принадлежностями (см. Приложение на 1 листе)Комплектация BD 8500: 1. Электронный блок 2. Манжета 3. Коробка для прибора Комплектация BD 8700: 1. Электронный блок 2. Манжета с резиновой трубкой 3. Блок питания для работы от сети 4. Коробка для прибора
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o67688
- Registration Number
- ФС № 2006/332
- Registration Date
- March 22, 2006
- Validity Period
- March 22, 2016
- Manufacturer Name (English)
- Bremed Italia s.r.l.
- Manufacturer Name (Russian)
- Bremed Italia s.r.l.
- Country (English)
- Italy
- Country (Russian)
- Италия
- Legal Address (English)
- Italy
- Legal Address (Russian)
- Италия
Access comprehensive regulatory information for Devices for measuring blood pressure and pulse rate digital automatic models BD 8500 BD 8700 with accessories (see Appendix on sheet 1)Equipment BD 8500: 1. Electronic unit 2. Cuff 3. Box for the device Equipment BD 8700: 1. Electronic unit 2. Cuff with rubber tube 3. Power supply for mains operation 4. Box for the appliance in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФС № 2006/332 and manufactured by Bremed Italia s.r.l.. The device was registered on March 22, 2006.
This page provides complete registration details including device type, manufacturer information, country of origin (Italy), 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.