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4. Warnings and precautions for users
•
The RIDASCREEN® Foodscreen Blood Collection Kit should be stored dry in the
original packaging between 9°C and 30°C.
•
The laboratory must receive your sample within two weeks from the date of
collection.
•
Do not use this kit for blood withdrawal if you are taking blood thinning
medications or if you have a blood clotting disorder unless you consult your
physician or therapist.
•
The lancets provided are sterile, single-use lancets. Once the finger is
punctured, the blade is automatically retracted into the sheath for safety.
•
The lancets have a puncture depth of 2.0 mm. Caution is advised for use on
young children: The distance between the finger surface and the bone may not
be sufficient and using the lancet could result in injury. Consult your physician
or therapist.
•
Use in children under the age of one year is not recommended.
•
Do not use open or damaged kits to collect blood.
•
The RIDASCREEN® Foodscreen Blood Collection Kit may not be used after the
expiration date on the package.
•
All the components in the kit are for single use only.
•
Anyone helping you take the blood sample should wear disposable gloves (not
contained in the kit).
•
Do not take blood samples from a finger with visible injuries, the earlobe, or the
little finger.
•
Keep away from children. Minors should not use the kit without parental
consent.
•
If you do not understand the instructions, please consult your physician or
pharmacist.
•
Users are responsible for the proper disposal of all materials after use. For
disposal, please adhere to national regulations.
•
R-Biopharm AG expressly rejects any liability for the use or sale of the
RIDASCREEN® Foodscreen Blood Collection Kit or its components if used for
anything other than the intended use specified in the instructions.
•
The RIDASCREEN® Foodscreen Blood Collection Kit is an accessory for the
RIDASCREEN® Spec. IgG Foodscreen and RIDACHIP® FoodGuide test systems
and was validated with them. R-Biopharm AG assumes no liability for use with
non-validated test systems.
•
For users in the European Union: Report all serious adverse events associated
with the product to R-Biopharm AG and the appropriate national authorities.
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