MEDICAL RECORDING PAPERS
INSTRUCTIONS
APPLICATION: medical recording papers are projected to
recorder traces of physiologic parameters of medical
equipments during diagnostic analysis.
Use is reserved only at medical and paramedical authorized
operators with competence in medical recording
equipments.
PRODUCT IDENTIFICATION:
The identification data ( device code, LOT production and
mark) are in the identification label stuck on the external
packaging.
USE AND INSTALLATION:
Before using this medical device it is always
necessary to control that paper size and paper grid (if
present) are concerning the use of the instrument.
Avoid the use of cutting tools in packaging opening.
Before using this medical device it is always
necessary to consult the instructions concerning the use of
the instrument.
Paper (roll or z-fold) has to be placed comfortable
in the paper hold of the instruments in order to not obstruct
paper dragging. Never force paper introduction in the
instrument.
The grid, if present and except any different
indication, use the mm unit and ±1% precision.
STORAGE CONDITIONS:
Before use,
store the paper in a fresh and dry place.
Long exposures to condensate and temperature higher or
lower than what indicated in label could cause adverse
effects to the paper.
Avoid the exposures to direct sunlight, bright lights (UV).
After registration,
to assure long time recording preservation:
Store the paper in a cool and dry place after use.
Avoid the exposures to direct sunlight, bright lights (UV).
Avoid any contact with liquids and solvents such as
alcohol, ketone, ligroin or similar.
Avoid any contact with other kind of chemical and thermal
paper.
Do not insert the paper in any envelopes made of PVC ,but
use qualified envelopes.
DISCHARGING CONDITIONS
Use, storage and discharging of the paper do not cause any
environmental pollution.
Papers discharging can be made in the appropriate boxes
for recycling.
The inflammability of this product is similar to normal
uncoated papers. To extinguish incidental fires of this
product use water or normal fire-extinguisher.
CONTRAINDICATIONS:
On the basis of previous experiences and several analysis
results, a correct use of the product cannot cause any
noxious effect.
REPORTS:
All serious accidents concerning the medical device
supplied by us must be reported to the manufacturer and
competent authority of the member state where your
registered office is located.
LUMED srl - Via Staffora, 18/9 20073 Opera (MI)
rev3.6 – 19/10/2022
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