Notification Form for incidents

If you experience a reportable incident (1), you have to fill out this online form. Messages through another delivery path will not be accepted. Your report will be edited as soon as possible.

Reporter Data


Person to contact*

Street, No.*

Zip, City*


Phone No.*



Date of incident*

Place of incident*

Part No.*

Lot-/Serial No.

Equipment used with product

Description of incident*

Injury to person(s)?*

Already reported to any other authority?*

The data sent will be processed only for the purpose of answering your request. Further information can be found in our privacy policy.

* Required fields to answer your request.
(1) An incident according to “§ 29 Medical device act or § 2 sec.1 Ordinance on Medical Devices Vigilance of Germany ” is any malfunction, any failure or deterioration in the characteristics or performance of a medical device as well as any inaccuracy in the labelling or instructions for use which has led, or could have led, directly or indirectly, to the death or serious deterioration in the state of health of a patient or user or another person.