Table of contents Table of contents 1. Important information ............................2. Foreword ................................. 3. Understanding these operating instructions .................... 4. Symbols in use ..............................5. Safety instructions and user obligations ..................... 6. Proper and intended usage ..........................7. Rating plate................................8.
All rights under the copyright law are expressly reserved for medifa. medifa is only responsible for the safety characteristics within the scope of the statutory regulations if all maintenance, servicing and changes to this device have been carried out by the user or a representative as instructed.
The medifa products are manufactured to have a long and trouble-free lifespan. The development, design and production at medifa have been certified to comply with DIN EN ISO 9001 and DIN EN ISO 13485. These products comply with the requirements of the Medical Devices Act and bear the CE mark.
Understanding these operating instructions 3. Understanding these operating instructions ATTENTION Please read and observe these operating instructions. This operating instructions must have been read and understood fully by the operating personnel before initially commis- sioning the product, this applies particularly to the chapter Safety instructions and user obligations. If necessary, in-house training for technical qualifications may be carried out by a qualified person.
Symbols in use 4. Symbols in use These operating instructions use various warning, notice and safety symbols to highlight information of particular relevance. Safety instructions DANGER DANGER indicates a hazardous situation which, if not avoided, will result in death or serious injury. WARNING WARNING indicates a hazardous situation which, if not avoided, could result in death or serious injury.
Repairs Repairs may only be carried out by the medifa technical support or by personnel who have been authorized, trained and cer- tified by medifa.The company medifa is not liable for any damages due to neglected inspections, inadequate repair, improper maintenance or changes made to the product! For servicing work, please contact the medifa technical support department.
Proper and intended usage 6. Proper and intended usage This product is an arm rest. It is an accessory of the medifa 8000. The medifa 8000 and the standard accessories are intended exclusively for human medical purposes. The product is intended for supporting and positioning the patient’s arm immediately before, during and after performing surgery as well as for examination and treatment.
Rating plate 7. Rating plate medifa GmbH & Co. KG Industriestraße 5 57413 Finnentrop, Germany 81220_x xxxxx MM/YYYY Fig. 1: Ratings plate 81220_x Elements / symbols Description Manufacturer specifications and contact information Article number Batch number QR code Date of manufacture Max.
Assembly and adjustment 8. Assembly and adjustment Inspection of the product for damage Make sure that all parts of the product are mechanically in order. The plastic parts must not have sharp edges or any kind of damage. Attaching the arm rest Press the clip-on retainer together and hook it (from Release the clip-on retainer The arm rest is now firmly top to bottom) into the carbon rail at the desired...
Care instructions 9. Care instructions CAUTION Risk of personal injury! Only cleaned and disinfected products and devices may be handed over to a service technician for maintenance and repair work! ATTENTION Danger: incorrect care may damage property! • Improper cleaning products can damage the surface! •...
The arm rest and packaging must be recycled in an environmentally friendly manner. The disposal of individual parts must also be carried out in an environmentally friendly manner (i.e. according to the relevant legal regulations)! For more information about the proper disposal of used products, please contact medifa Technical Support, your local dealer or the appropriate national authority.
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