10.
Guarantee
TThe performances of the Pressio® monitoring kit are only guaranteed with
the range of Pressio® monitoring systems and the accessories designed,
tested and manufactured by Sophysa.
Sophysa guarantees that this medical device is free from defects in material
or manufacturing. Apart from this guarantee, Sophysa does not grant any other
guarantee, express or implicit, including marketing or adaptation for a specific
use. Sophysa cannot be held responsible for any incident, complication, damage
or prejudice resulting directly or indirectly from the use of this device. Sophysa does
not authorize anyone to take responsibility on its behalf for its products.
11.
Processing of the products after use
Destruction after use
An unpacked, used or explanted Pressio® monitoring kit must be destroyed
in accordance with the procedures in force in the medical establishment.
Return of products
If an explanted Pressio® monitoring kit needs to be returned to Sophysa for analysis,
indicating if necessary whether cleaning has been performed.
In order to assess the returned product properly, it must be accompanied
by an explanatory Return to Manufacturer Authorization form.
N
:
otes
f
,
oR moRe effective analysis
it is Recommended that the device is not cleaned
i
p
®
n the case of a
Ressio
paRenchymal kit with bolt
.
caRefully
12.
Symbols
Catalog reference
Manufacturer
Sterilization Method using Ethylene Oxide
Do not re-use
Do not re-sterilize
Use until
Batch code
L OT
Serial number
CE Conformity Marking
.
,
Remove the catheteR fRom the bolt
10/74
Refer to the instructions for use
BF TYPE EQUIPMENT: Procuring an appropriate
degree of protection against electric shock,
having a Type F insulated applied section
(floating).
Temperature conditions for storage and
transport
Store in a dry place
Fragile, handle with care