St. Jude Medical PressureWire Aeris, Instructions For Use Manual

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15
Equipment includes RF transmitter.
Electrostatic sensitive device.
Do not use if package is damaged.
For single use only. Do not reuse.
S TERILIZE
Do not resterilize.
STE RILE EO
Sterilized using Ethylene Oxide.
Electronic waste bin. Disposal according to EU´s Battery Directive 2006/66/EC.
Electronic waste bin. Disposal according to EU´s WEEE Directive 2002/96/EC.
PressureWire Aeris complies with the Medical Device Directive 93/42/EEC and
Radio and Telecommunication Terminal Equipment Directive 1999/5/EC.
USA only: Federal law restricts this device to sale by or on the order of a Physician.
FCC ID:
IC ID:
FCC identifier for the transmitter.
IC identifier for transmitter.
This device complies with part 15 of the FCC Rules and RSS-210 of the IC 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.
C-tick compliance with AS/NZS 4268.
Japanese RF identifier for the transmitter.
KCC identifier for the transmitter.
Made in Sweden
Made in Sweden.
Made in Costa Rica
Made in Costa Rica.
Flush packaging coil with saline.
CONNECT
Connect.
Switch on Aeris transmitter.