Canon CR-2 PLUS AF Manuel d'utilisation - Page 4

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1. Basic Operations
2. Troubleshooting

Safety

Regulatory Information

CE marking

This device complies with the following:

• Regulalation (EU) 2017/745

• Directive 2011/65/EU

For European Union

Notification of Serious Incident

Any serious incident (defined in Article 2(65) of the Regulation (EU) 2017/745) that has occurred in

relation to the device should be reported to the manufacturer and the competent authority of

the Member State in which the user and/or patient is established.

Electronic Instructions for Use

Instructions for use are available on the website for viewing and download by customers.

• https://global.canon/en/ifu/medcom/index.html

For details, please contact your sales representative or local Canon dealer.