Philips TRANSPAC 4 Bedienungsanleitung Seite 5

LIST NO. 453564326511
COMMODITY NO. DF-4520
DATE PREPARED 1-26-2012
ARTIST KENT
C. Activate pump delivery mechanism to pump solution through the flush device while
allowing arterial cannula to back flow during attachment.
CAUTION: Be certain not to introduce air into the system during connection
procedure.
CAUTION: If this product is used with fat emulsions, they must be introduced
through the lipid compatible stopcock that is distal to the flush transducer
assembly to avoid cracking of the transducer line.
VI. Checking For Leaks
After approximately one minute has elapsed the flow rate should be observed at the
drip chamber to ensure that the continuous flush device is operating properly. A visual
inspection for leaks should also be made since a small leak can misrepresent the actual
continuous flow through the catheter. A protocol should be established according to
the hospital standard of care for routinely checking the system for proper fluid source
pressure, flow rate and leaks.
VII. Indications and Contraindications
A. Indications
● Umbilical artery catheterization of neonates
● Invasive pressure monitoring with infusion pump
B. Contraindications
● Left atrial monitoring without an air-eliminating filter between the solution source
and continuous flush device
● Intracranial pressure monitoring
● Compartmental pressure monitoring
● Intrauterine pressure monitoring
DO NOT USE A PRESSURE ADMINISTRATION CUFF.
THE TRANSPAC 4 KIT IS A SINGLE USE DEVICE. DO NOT REUSE. REUSE
®
NEGATIVELY IMPACTS PERFORMANCE / STERILITY POTENTIALLY RESULTING IN
PRODUCT FAILURE/ CONTAMINATION.
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PAPER AND INK SPECS: REFER TO SPECIFICATION IS-012
FINISHED TRIM: 8.5" X 11" (± 1/8")
FINISHED FOLD: 4.25" x 11" (± 1/8")
VENDOR TO CERTIFY PAPER STOCK
VENDOR: SEE SPECIFICATION IS-012
EN