
SpiroSphere
®
ECG Instructions for Use
Page 106/136
Version 02.02 • 04AUG2022
The following applies to products that are potentially contaminated by biological working substan-
ces of risk group 3 and 2 according to the regulation on biological substances and that are thus
classi ed as Transport Category B:
Please contact ERT
before
returning the goods and observe the regulations for the transport of
dangerous goods.
2. Cleaning
If the products had contact with biological working substances (for example blood or other body
uids), they have to be cleaned and disinfected in a combined cleaning and disinfection procedu-
re, unless a differing agreement has been made with ERT.
As a rule, the products also have to be cleaned in order to minimize adhesions and bacterial
contamination. Unless body uids, tissue or contrast agents etc. have caused the product to be
defective, deposits and adhesions should be removed carefully without damaging or altering the
product, if possible. For this, refer to the notes on the preparation of products.
Products which have been contaminated by highly active pharmaceuticals have to be cleaned
appropriately with tap water.
3. Disinfection/Sterilization
After cleaning, the products have to be disinfected and/or sterilized (only if
permitted for this medical product) in order to avoid harm to your and our
employees.
If in doubt or in case of suspected material incompatibility, please consult ERT.
4. Packaging
To avoid any contamination, the cleaned and disinfected product has to be packed as follows:
a) Put it into a sealable primary packing.
b) Put the primary packing in a waterproof secondary packing (if possible use hard packing
material).
c) Pack the secondary packing with a neutral packing material.
For “
Packaging and labeling of non
contaminated products
“: see point 6.
If in doubt, contact ERT for guidance on further actions!
Parts with sharp edges need to be packed particularly safe.
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