pajunk StimuLong Plus Gebrauchsanweisung Seite 10

Instructions for Use
Special notice
Please read the following information and operating instructions carefully.
Caution: Federal law restricts this device to sale by or on the order of a physician.
Rx
only
The device may only be used by qualified medical staff in accordance with
these user instructions.
PAJUNK® does not recommend any particular treatment method. Professional
medical staff are responsible for the way in which the device is used and for
patient selection.
Failure to comply with the user instructions invalidates the warranty and puts
patient safety at risk.
If used in combination with other products, it is essential that the compatibility
information and user instructions for these other products are taken into account.
A decision regarding the combined use of devices from different manufacturers
(where they do not constitute treatment units) is the responsibility of the user.
The device must not be used under any circumstances if there are good
reasons to suspect incompleteness, damage or loss of sterility.
Only devices in perfect condition, which are within the sterile expiry date
marked on the label, in undamaged packaging, may be used.
Device description/ compatibility
Please see the current declaration of conformity for product numbers and
the scope of these instructions for use.
StimuLong Plus/ StimuLong NanoLine/ SimuLong Sono are provided by
PAJUNK® in convenient kits consisting of:
• Cannula: PlexoLong NanoLine with echogenic Cornerstone stamps
• Stimulong Catheter (with/ without stylet, with/ without helical coil) in cath-
eter container
• Stimulong ClampingAdapter/ Clamping adapter
• Sealing cap
• Filter bacterial filter 0,2 µm
• FixoLong filter/ catheter fixation
• FixoCath catheter fixation
• Adapter cable/ intermediate cable
Hub connectivity: LUER
The exact composition may be gathered from the label.
The catheter, cannula and all relevant components may not be used for
more than 72 hours.
Please note that the continued use of a device of the same type must be assessed
cumulatively as described in the legislation on medical devices, even after the
device has been exchanged or replaced.
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