Symbols Glossary - Philips RESPIRONICS System One User Manual

The use of positive airway pressure therapy may be temporarily contraindicated if you exhibit signs of
a sinus or middle ear infection. Not for use with patients whose upper airways are bypassed. Contact
your health care professional if you have any questions concerning your therapy.
Refer to the instructions for use that accompanied your therapy device for any additional
contraindications that may be specific to the use of that device.

Symbols Glossary

The following symbols may appear on this device and its packaging. Refer to http://www.symbols.
philips.com for a description of the symbols used on this device and its packaging.
S
ymbol
Catalogue number
Indicates the manufacturer's catalogue
number so the medical device can be
identified.
Serial number
Identifies the manufacturer's serial
number for the medical device.
Medical Device
Indicates that the item is a medical device.
Unique Device Identifier
Indicates the Unique Device Identifier
information.
Manufacturer's number
Humidity limitation
Indicates the range of humidity to
which the medical device can be safely
exposed.
Temperature limitation
Indicates the storage temperature limits
to which the medical device can be
safely exposed.
Manufacturer
Indicates the medical device
manufacturer.
Date of Manufacture
To indicate the date on which a product
was manufactured.
US
Country of Manufacturer
To indicate the country of manufacture
of the product.
4
D
efinition
S
ymbol
Operator's manual; Consult
accompanying instructions for use.
Packaging unit
To indicate the number of pieces in the
package.
Authorized Representative in the
European Community
Maximum Fill Line
Warning: Hot Water, Hot Surface
Drip proof equipment
Protection against ingress of solid
foreign objects ≥ 12.5 mm diameter.
Protection against ingress of water with
harmful effects dripping (15° tilted).
Type BF applied part
To identify a type BF applied part
complying with IEC 60601-1.
Separate collection for electrical and
electronic equipment per EC Directive
2012/19/EU.
MR Unsafe
Do not use device in a Magnetic
Resonance (MR) environment
D
efinition