8
1
General Information
1.1
Manufacturer
We thank you for buying one of our products.
This product bears the CE mark. This means that it meets the basic requirements on the safety and the
performance of medical devices set forth by the respective applicable European regulations.
We are the manufacturer of this product:
Gebrüder Martin GmbH & Co. KG
A company of the KLS Martin Group
KLS Martin Platz 1 · D-78532 Tuttlingen · Germany
P.O. Box 60 · D-78501 Tuttlingen · Germany
Phone +49 7461 706-0 · Fax +49 7461 706-193
[email protected] ·www.klsmartin.com
1.2
Hotline
Should you have any questions on how to handle the device or product or use it for clinical applications,
please do not hesitate to contact the Product Management:
Phone: +49 7461 706-321
Fax:
+49 7461 706-190
In case of technical questions and questions regarding maintenance contracts and training, please contact
our Martin Service Center:
Phone: +49 7461 706-343
Fax:
+49 7461 706-484
E-mail: [email protected]
To answer your technical questions as efficiently as possible, our service technicians require the catalogue
number (REF), serial number (SN) and the manufacturing date ( ) of the product. All this information can
found on the rating plate; see section 14.3 “Rating Plate and Serial Number”, page 136.
1.3
Obligation to Report Incidents
All serious incidents occurring in connection with the product must be reported to Gebrüder Martin and
the respective authorities without delay.
