Product Complaints
Any health care professional (for example a customer or a user) who has any
complaints or has experienced any dissatisfaction with the quality, durability,
reliability, safety, effectiveness, or performance of this product must notify
Agfa.
For a patient/user/third party in the European Union and in countries with
identical regulatory regimes (Regulation 2017/745/EU on Medical Devices);
if, during the use of this device or as a result of its use, a serious incident has
occurred, please report it to the manufacturer and/or its authorised
representative and to your national authority.
Manufacturer address:
Agfa Service Support - local support addresses and phone numbers are listed
on www.agfa.com
Agfa - Septestraat 27, 2640 Mortsel, Belgium
Agfa - Fax +32 3 444 7094
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| DR 800 | Product Information
0392C EN 20210309 1049
Summary of Contents for 6010/200
Page 1: ...DR 800 6010 200 User Manual 0392C EN 20210309 1049 ...
Page 95: ...DR 800 Safety Directions 95 0392C EN 20210309 1049 ...
Page 116: ...Resetting the fluo timer on page 203 116 DR 800 Basic Workflow 0392C EN 20210309 1049 ...
Page 123: ...DR 800 Basic Workflow 123 0392C EN 20210309 1049 ...
Page 217: ...Patient size mAs Extra Large normal mAs 4 DR 800 Software Console 217 0392C EN 20210309 1049 ...