Ambit PIB v1.5 - Page 7

Section 1 • Introduction
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Indicatesthemedicaldevicemanufacturer,asdenedinEUDirectives
90/385/EEC, 93/42/EEC and 98/79/EC.
Indicates the date after which the medical device is not to be used.
Indicates the manufacturer’s batch code so that the batch or lot can be
identied.
Indicatesthemanufacturer’sserialnumbersothataspecicmedical
devicecanbeidentied.
Single-use only (cassettes)
Keep away from heat
Keep dry
Caution:Thisdeviceisrestrictedtosalebyorontheorderofa
physician.
Temperature limitation
Sterilized using irradiation
DEHP-freeuidpath
Notmadewithnaturalrubberlatex