Nantlife BP4.0 User Manual - page 16
English
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Power supply
4 alkaline 1.5V AAA batteries
Battery Life
Approximately 300 uses starting with new alkaline batteries when
inflated to 170mmHg at 73°F (23°C) with standard adult cuff
Unit dimensions
185mm x 138mm x 100mm 7.3” x 5.4” x 4”
Weight
980g (34.5oz) not including batteries
Note: These specifications are subject to change without notice.
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Manufacturer
Manufactured by NantCare LLC - Made in China
Distributed by NantCare LLC dba NantLife
2929 N 44th Street - Phoenix, Arizona 85018
Toll free phone 1-855-NANTCARE www.NantLife.com
The manufacturer has calibrated the device for a period of two years. Metrological inspection and adjustment must take place of two
years. Metrological inspection and adjustment is subject to a fee and can be carried out by NantLife, a responsible authority, or an autho-
rized maintenance service.
NantLife certifies that:
(SP10) we need to choose depending on the type of evaluation we did. VJ
For devices validated against indirect cuff/stethoscope, trained-observer auscultation, the statement shall
be worded in the following or substantially equivalent language: “Blood pressure measurements
determined with the NantLife Blood Pressure Monitor are equivalent to those obtained by a trained observer using the
cuff/stethoscope auscultation method, within the limits prescribed by the American National Standard,
Electronic or automated sphygmomanometers.” OR
For devices validated against intra-arterial measurements, the statement shall be worded in the following
or substantially equivalent language: “Blood pressure measurements determined with the NantLife Blood Pressure Monitor are equiva-
lent to those obtained by an intra-arterial blood pressure measurement device, within the limits prescribed by the American National
Standard, Electronic or automated sphygmomanometers.”
OR BOTH For devices validated against both methods, these two statements may be combined.
The NantLife Smart Blood Pressure Monitor meets the relevant provisions of the Council Directive 93/42/EEC of 14 June 1993 concerning
medical devices.
The measuring accuracy meets the requirements of the European Society of Hypertension (ESH) and British Hypertensio0n Society (BHS).
Stolberg, October 2008
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