requirements for electro-mechanical blood pressure
measuring systems) and IEC 80601-2-30 (Medical
electrical equipment – Part 2–30: Particular requirements
for the safety and essential performance of automated
noninvasive blood pressure monitors).
• The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life. If using the device for commercial medical
purposes, it must be regularly tested for accuracy by
appropriate means.
13. Power Supply Unit
Input
100 – 240 V, 50 – 60 Hz
Output
6 V DC, 600 mA, only in connection with
this Beurer blood pressure monitor.
Protection
This device is double insulated and
protected against short circuit and
overload by a primary fuse.
Make sure to take the batteries out of
the compartment before using the mains
part.
Polarity of the the DC voltage connection
Double insulated / equipment class 2
Enclosures and
Equipment enclosed to protect against
Protective
contact with live parts, and with parts
Covers
which can become live (finger, pin, hook
test).
The operator shall not contact the patient
and the output plug of AC mains part
simultaneously.
14. FCC Compliance Information
Upper Arm Blood Pressure Monitor BM 28
Responsible Party – U.S. Contact Information
Beurer North America LP
1 Oakwood Boulevard, Suite 255
Hollywood, FL 33020
United States
1-800-536-0366
FCC Compliance Statement
This device complies with Part 15 of the FCC Rules.
Operation is subject to the following two conditions:
(1) this device may not cause harmful interference, and
(2) this device must accept any interference received,
including interference that may cause undesired
operation.
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