Instrument for measuring blood pressure and pulse rate digital semi-automatic model BD 8600 with accessories (see Appendix on 1 sheet)Equipment BD 8600: 1. Electronic block 2. Cuff 3. Rubber tubes 4. Pneumosupercharger 5. Air bleed valve 6. Power supply for mains operation 7. Box for the appliance
Russia·Unknown·Bremed Italia s.r.l.·Registered March 22, 2006·N/A- Device Name (English)
- Instrument for measuring blood pressure and pulse rate digital semi-automatic model BD 8600 with accessories (see Appendix on 1 sheet)Equipment BD 8600: 1. Electronic block 2. Cuff 3. Rubber tubes 4. Pneumosupercharger 5. Air bleed valve 6. Power supply for mains operation 7. Box for the appliance
- Device Name (Russian)
- Прибор для измерения артериального давления и частоты пульса цифровой полуавтоматический модель BD 8600 с принадлежностями (см. Приложение на 1 листе)Комплектация BD 8600: 1. Элекронный блок 2. Манжета 3. Резиновые трубки 4. Пневмонагнетатель 5. Клапан для стравливания воздуха 6. Блок питания для работы от сети 7. Коробка для прибора
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o67689
- Registration Number
- ФС № 2006/333
- 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 Instrument for measuring blood pressure and pulse rate digital semi-automatic model BD 8600 with accessories (see Appendix on 1 sheet)Equipment BD 8600: 1. Electronic block 2. Cuff 3. Rubber tubes 4. Pneumosupercharger 5. Air bleed valve 6. Power supply for mains operation 7. 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 № 2006/333 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.