pajunk PlexoLong NanoLine Manual Del Usuario página 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.
In addition to these instruction for use, the relevant information also applies
according to the corresponding specialist literature and current state of the art
and knowledge.
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.
Product specification / compatibility
Please see the current declaration of conformity for product numbers and the
scope of these instructions for use.
PlexoLong NanoLine/ SonoLong NanoLine are provided by PAJUNK® in conve-
nient kits consisting of:
• Cannula: PlexoLong NanoLine/ SonoLong NanoLine with echogenic Corner-
stone stamps
• PlexoLong Catheter/ SonoLong Catheter (with/without stylet, with/without
helical coil) in container
• Clamping Adapter
• Catheter container
• Sealing/locking cap
• Haemostylet
• Filter bacterial filter 0,2 µm
• FixoLong filter/catheter fixation
Hub connectivity: LUER or
10