IFU-SalivaEjectors-A4-GB-2407-EN

3. PRODUCT PACKAGING AND LABELING The product is packed in non-sterile bags of 100 or 250 pieces. Each package is equipped with specific labeling. 4. INFORMATION ABOUT CONNECTING WITH OTHER DEVICES The device must be connected to the common saliva suction system used in the medical-dental environment. There are no accessories or connection to other devices. 5. LIMITS OF LIABILITY The construction of the product is particularly aimed at ensuring a high degree of operational safety, within the limits set by these instructions for use. The manufacturer assumes no liability in the event of use of the product in the conditions hereinafter considered as improper use:

• Anything not specifically covered by the instructions • Failure to comply with the manufacturer’s prescriptions • Total or partial non-compliance with the instructions • Inappropriate storage • Use for purposes other than that set for the device

6. REPORTING OF SERIOUS ACCIDENTS Report any serious incident in relation to the device to the manufacturer and the competent authority of the Member State where the user and / or patient is established.

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