pajunk NerveGuard NRFit Gebrauchsanweisung Seite 6

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.
Device description/ compatibility
• NerveGuard, green,
18 G -22 G
• NerveGuard, purple,
24 G -25 G
According to current information, a high injection pressure is a reliable warning
sign for intrafascicular nerve injections. The risk of nerve injuries increases in line
with rising injection pressure in the case of peripheral nerve blocks of the upper
and lower limbs.
"NerveGuard" prevents injections being given at excessive pressure. The flow of
the local anesthetic solution is automatically blocked by a valve.
Hub connectivity:
Dead space volume max. 1 ml
Compatible with the 5-20 ml syringes and PAJUNK
cations.
In addition to these instructions for use, the relevant information also
applies according to the corresponding specialist literature and current
state of the art and knowledge.
6
(Art. No. 001163-38M) for cannula diameters
(Art. No. 001163-38N) for cannula diameters
cannula for peripheral appli-
®