of the Manu-
The devices are intended to be used in a hospital environment and for
transport monitoring by trained health care professionals inside and
The devices are not intended for home use.
This is not a therapeutic device.
The Philips M3046A Compact Portable Patient Monitor
complies with the requirements of the Council
Directive 93/42/EEC of 14 June 1993 concerning
medical devices and carries CE marking accordingly.
The system also complies with the Council Directive 1999/5/EC of 9
March 1999 concerning radio equipment and telecommunications
terminal equipment. The following symbol, CE(!), means that this
device is considered Class 2 radio equipment per Directive 1999/5/EC
for which Member States may apply restrictions on putting the device
into service or placing it on the market. This system is intended to be
connected to the publicly available interfaces (PAI).
This product is Class 2 under the scope of the R&TTE. Be aware that
France and Spain use frequencies other than those of the rest of the
EEA. This means that products bought elsewhere might cause
problems in France and Spain and should be avoided
Philips Medical Systems only considers itself responsible for any effects
on safety, reliability and performance of the equipment if:
assembly operations, extensions, re-adjustments, modifications or
repairs are carried out by persons authorized by Philips Medical
the electrical installation of the relevant room complies with
national standards, and
the instrument is used in accordance with the instructions for