Instructions for Use
IPS® Implants Forearm Reconstruction
2.4
Inspection upon Receipt by User
• Immediately upon receipt, the goods must be checked for completeness and potential damage in transit.
• In particular, the original packaging and, if applicable, the packaging seal or the protective foil must be
checked for absence of damage.
• Any transport damage as well as deviations from the delivery note must be reported immediately.
• Inspect the delivery on the basis of the case planning documentation in your possession. This is ideally
done based on the case number. If these data do not match the documentation on hand, there has been
a mix-up, and the product must not be used.
2.5
Warranty
Our Standard Terms and Conditions of Sale as most recently amended shall apply. Agreements diverging
from these Standard Terms and Conditions do not restrict the legal rights of the buyer.
Any additional warranty exceeding the above provisions must be in contractual form and shall exclude
consumables and product-related vandalism.
To avoid damage from improper use and not to compromise the warranty or guarantee, the
Gebrüder Martin implant system must not be used in combination with implant systems by other
manufacturers.
The system-relevant products may be repaired only by Gebrüder Martin or a qualified person or company
expressly authorized by Gebrüder Martin to perform such work.
The treating physician is responsible for the use of patient-specific products and for the clinical planning.
The design/implementation of the product must be based on the current state of the art, e.g. regarding
material strength. Special cases that require deviations, in particular due to the anatomical circumstances,
must be explicitly coordinated
Danger of injury and risk of system failure!
Before their use in a surgical environment, patient-specific products must be subjected to a final
inspection by a qualified user under all circumstances. This user must be familiar with the entire planning
process and the pre-surgical consultation.
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