1.3 User groups
This product may only be used by qualified, expert personnel. A prerequisite is theoretical
and practical experience in handling the scoop stretcher.
1.4. Declaration of conformity
The scoop stretchers conform to the DIN EN 1865-1 standard and to the Medical Device
Regulation (EU) 2017/745. A declaration of conformity for these products can be acquired
from the local dealership or the manufacturer.
2. Information on the safety and protection of the product
1. Before and after every use, check the components and patient
restraining belts for damage and completeness.
2. Ensure that the patient restraining belts are correctly installed.
3. Before initial use, conduct a test run with an empty
scoop stretcher
to
become aware of the handling of the product.
4. In the event of damage or suspected damage to the straps or the scoop
stretcher, remove the product from operation immediately until any
occurring irregularities have been remedied.
5. All serious incidents related to the device shall be reported to the
manufacturer and to the competent authority of the Member State
where the user and/or the patient is established.
3. Purpose and use of the scoop stretcher
The ultraSCOOP STRETCHER (X-RAY) is a scoop stretcher for motionless repositioning,
immobilisation and transport of injured persons who may have suffered a spinal fracture.
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