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AGFA DX-M - Training; Product Complaints

AGFA DX-M
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14
2321 E EN 20130722
DX-G/DX-M
Training
The user must have received adequate, Agfa certified training on the safe and
effective use of the product before attempting to work with it. Training
requirements may vary from country to country. The user must ensure that
training is received in accordance with local laws or regulations that have the
force of law. Your Agfa certified representative can provide further
information on certified training.
The user must note the following information in the preliminary section of
this manual:
“Intended Use” on page 12.
“Intended User” on page 12.
“Safety Directions” on page 43.
Product Complaints
Any health care professional (for example a customer or a user) who has any
complaints or has experienced any dissatisfaction in the quality, durability,
reliability, safety, effectiveness or performance of this product must notify
Agfa.
If the device malfunctions and may have caused or contributed to a serious
injury of a patient, Agfa must be notified immediately by telephone, fax or
written correspondence to the following address:
Agfa Service Support - local support addresses and phone numbers listed on
www.agfa.com
Agfa HealthCare N.V. - Septestraat 27 - 2640 Mortsel, Belgium.
Agfa HealthCare N.V. - Fax +32 3 444 7094.

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