Fresenius Medical Care Ci-Ca Dialysate K2 Instructions D'utilisation page 5

Ci-Ca Dialysate K2 Ci-Ca Dialysate K2
be confirmed by measuring the citrate-induced drop of the
ionized calcium concentration in the extracorporeal circuit
no later than 20 – 30 minutes after the start of the treatment.
If this drop is missing, the set-up must be re-checked as
mixing-up of the citrate and calcium infusion can lead to
severe electrolyte imbalance and acid-base disturbance.
- The treating physician is responsible for any substance
that is added to the unmixed or mixed solution. The
compatibility of the substance must be checked beforehand
to avoid undesirable effects such as particle formation. After
admixture, the solution must be mixed again.
- Any unused portion of solution is to be discarded.
Additional technical warnings and precautions may be specific
to other devices or drugs used in the therapy.
PARTICULAR NOTES ON MATERIALS
AND SUBSTANCES
There is no hypersensitivity to the bag system or any of the
materials known.
For SVHC information according to Article 33 of Regulation
(EC) No. 1907/2006 ("REACH"), please use this page:
www.freseniusmedicalcare.com/en/svhc
SPECIAL PRECAUTIONS FOR
STORAGE
Keep away from sharp objects such as knives and scissors.
Do not store below +4 °C or above +25 °C.
Keep dry.
DISPOSAL
Ensure safe disposal of any unused product or waste material
in accordance with local regulations.
Materials that have been in contact with blood or other
material of human origin may be infectious. Dispose of such
materials by taking the necessary precautionary measures and
in accordance with local regulations for (potentially) infectious
materials.
SYMBOLS USED ON LABELS
Sterilized using steam
Catalogue number
Medical Device
Manufacturer
Use-by date
Single sterile barrier system with
protective packaging outside
Patient information website
Units
Temperature limit
Batch code
Unique Device Identifier
UDI
Date of manufacture
Caution
Do not re-use
Consult instructions for use
DATE OF REVISION OF TEXT
2022-05
A digital version of this document is available on the following
website:
www.freseniusmedicalcare.com/en/product-information
INFORMATION ON THE
MANUFACTURER
Legal manufacturer
Fresenius Medical Care AG & Co. KGaA
Fresenius Medical Care AG & Co. KGaA
Else-Kröner-Str. 1, 61352 Bad Homburg, GERMANY
D-61346 Bad Homburg ·
+49 6172 609-0
0123 0123
+49 6172/609-0
en