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BPM-260

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BPM-260

Product catalog summary

Specifications:

Color: White
Dimensions: 100.3 x 132.3 x 47.1 mm (length/width/height)
Weight: Approximately 273 g (excluding batteries and cuff)
Power Supply: 1.5V AAA alkaline batteries or AC Adapter (5V 1000 mA Class II ME Equipment)
Measurement Range: Systolic: 60-230 mmHg, Diastolic: 40-130 mmHg, Pulse: 40-199 BPM
Accuracy: Clinical validation with a mean difference within ±5 mmHg; Standard deviation ≤8 mmHg
Measurement Method: Oscillometric, detects blood movement through the brachial artery
Arm Circumference: Approximately 16-36 cm, 22-32 cm, 22-42 cm, or 22-45 cm
Memory: 2x199 readings
Communication Method: Bluetooth

Operating Environment:

Temperature: +5°C to +40°C
Relative Humidity: 15% to 90%, non-condensing
Atmospheric Pressure: 700 hPa to 1060 hPa

Storage Environment:

Temperature: -20°C to +60°C
Relative Humidity: <93%, non-condensing
Atmospheric Pressure: 500 hPa to 1060 hPa

Certifications:

CE Marking: Complies with Directive 2017/745 on Medical Devices Regulation (MDR), Annex IX Chapter I and III (Devices in Class IIa, IIb)
EC Certificate/Report No: G10 082800 0048 REV.00 / GZ2001422
RoHS Certificate: Complies with RoHS Directive (EU) 2015/863 amending Annex II to directive 2011/65/EU. Report No: CANEC23003018001

Catalog excerpts

LifeVit BPM-260 TENSIÔMETRO DE BRAZO INTELIGENTE |Color: Aprox.273 g (sin incluir baterias y manguito) IAC Adapter Powered Mode: 5V 1000 mA Class Il ME Equipment (SIS: 6OmmHg~230mmHg IDIA: 40mmHg~ 130mmHg Pulso: 40-199 BPM Presiôn estatica: 5°C-40°C dentro de +3mmHg Pulso: +5% alkaline batteries; Validaciôn clinica: Diferencia media dentro de +5mmHg; IDesviacién estandar s8mmHq (Oscilométrico. El dispositivo detecta el movimiento de la sangre a través de lal jarteria branquial, convirtiendo la presiôn sanguinea en una lectura digital. Med del perimetro del brazo upeñor: [Memoria: [Método de comunicaciôn: 2x199 Bluetooth Temperatura de: +5°C a +40°C Rango de Humedad relativa de 15% a 90%, no-condensada Presiôn parcial de vapor de agua no superior a 50 hPa. Entorno operativo: IRango de presiôn atmosférica de 700 hPa a 1060 hPa Temperatura:-20°C a +60°C Rango de humedad relativa < 93%, no-condensada, Presiôn parcial de vapor de agua no superior a 50 hPa. Entorno de almacenaje: IRango de presiôn atmosféricade 500 hPa a 1060 hPa EC CERTIFICATE Directive 2017/745 on Medical Devices Regulation (MDR), Annex IX Chapter | and III (Devices in Class Ila, IIb ). EC Certificate/ Report No: G10 082800 0048 REV.00 / GZ2001422 RoHS CERTIFICATE RoHS Directive (EU) 2015/863 amending Annex I to directive 2011/65/EU.

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*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.

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