Stryker 0711-001-000, Инструкция по эксплуатации

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1 1..5 5.. S Sa affe ettyy D Diirre eccttiivve ess
G Ge en ne erra all S Sa affe ettyy
W WA AR RN NIIN NG G -- Healthcare professionals should be thoroughly familiar with the instructions for use and the operation of
this product prior to use.
W WA AR RN NIIN NG G -- Healthcare professionals should be thoroughly familiar with the performance characteristics, and the
indicated, contraindicated, and intended uses of this product. Contact your Stryker sales representative or Stryker
Neptune Customer Service for in-service training.
W WA AR RN NIIN NG G -- The healthcare professional performing any procedure is responsible for determining the
appropriateness of this product and the specific technique used for each patient. Stryker, as a manufacturer, does not
recommend surgical procedure or technique.
M Ma ag gn ne ettiicc R Re esso on na an ncce e IIm ma ag giin ng g ((M MR RII)) S Sa affe ettyy
W WA AR RN NIIN NG G -- This product is MR unsafe. Do not use the product in an MRI environment. Operating the
product outside the specified environmental conditions could result in death or serious injury.
C Co on nn ne eccttiio on n S Sa affe ettyy
W WA AR RN NIIN NG G
IIN NA AP PP PR RO OP PR RIIA AT TE E C CO ON NN NE EC CT TIIO ON N H HA AZ ZA AR RD DS S
• Do not connect directly to chest tubes.
• Do not connect to closed wound drains.
• Do not connect directly to tracheal tubes.
• Not for use as a suction source for: intermittent suction applications, patient positioner devices, and organ stabilizer/
positioner devices.
Death or serious injury can result from inappropriate connections.
S Su uccttiio on n S Sa affe ettyy
W WA AR RN NIIN NG G
H HIIG GH H S SU UC CT TIIO ON N H HA AZ ZA AR RD D:: M MA AX XIIM MU UM M = = [[5 52 20 0 m mm m--H Hg g]]
• Always use the minimum suction limit range required to achieve the desired clinical outcome.
• Always follow your institution’s guidelines for suction limits.
• The effectiveness of aspiration is dependent upon the intensity of the suction applied.
• The suction limit range of the collection canister may be adjusted by using the suction control dial on the main control
panel. Interruption and restoration of rover power while suction is ON, whether accidental or intentional, does not
reset the suction limit range to zero. See BS EN ISO 10079-1: 2015 + A1: 2019, clause 9.11. Use caution when
activating suction with a high suction limit range.
Death or serious injury can result from improper suction levels.
700000969828 Rev-AA 5 EN
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