8
9
Date of manufacture, indicating the date when the device was
manufactured
Use-by date, indicating the date after which the device is not
to be used (i.e., the expiration date)
Batch code, indicating the manufacturing batch or lot number
Catalog number, indicating the catalog number so the device
can
Sterilized using ethylene oxide
Sterilized using irradiation
Do not resterilize, indicating that the device is not to be reste
-rilized.
Non-sterile, indicating that the device has not been subjected
to a sterilization process.
Do not use if package has been damaged or opened
Keep away from sunlight, indicating that the device should be
protected from light sources during storage
2
Keep dry, indicating that the device needs to be protected
from moisture during storage
Do not re-use, indicating that the device is intended for one
use, or for use on a single patient during a single procedure
Consult instructions for use.
5.1.3
5.1.4
5.1.5
5.1.6
5.2.3
5.2.4
5.2.6
5.2.7
5.2.8
5.3.2
5.3.4
5.4.2
5.4.3
operating conditions after it is stored either at the maximum or at the
minimum storage temperature. For additional information of operating and
storage/transport temperature.
• DO NOT crease the wrist cuff excessively.
• DO NOT use this monitor after the durable period has ended.
never apply the wrist cuffover a wound, as this can cause further injury;
• “WARNING: No modification of this equipment is allowed.”
• “WARNING: Do not modify this equipment without authorization of the
manufacturer.”
• “WARNING: If this equipment is modified, appropriate inspection and
testing must be
conducted to ensure continued safe use of the equipment.”
Symbol
Reference
Number
(ISO
15223-1)
Manufacturer, indicating the medical devices manufacturer as
5.1.1
Authorized representative in the European Community
5.1.2
The following symbols are adopted from ISO 15223-1 (Medical devices – Symbols to be used with
medical device
