General; Manufacturer; Hotline; Adverse Incident Reporting Requirement - KLS Martin group 90-254-58-10 Mode D'emploi

Monopolar Dental and Full Stainless Steel Electrodes
Instructions for Use

1 General

1.1

Manufacturer

Thank you for choosing a KLS Martin product.
This product has the CE mark, which means that it is compliant with the essential safety and performance
requirements for medical devices pursuant to 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
Tel. +49 7461 706-0 · Fax +49 7461 706-193
info@klsmartin.com · www.klsmartin.com
1.2

Hotline

Should you have any questions on how to handle the product or use it for clinical applications, please do
not hesitate to contact the Product Management:
Tel: +49 7461 706-243
Fax: +49 7461 706-190
If you have technical questions or questions about maintenance contracts and training, please contact the
Martin Service Center:
Tel: +49 7461 706-343
Fax: +49 7461 706-484
E-Mail: service@klsmartin.com
Each packaging and most products are marked with a specific lot number (LOT) and a reference number
(REF). When making a product complaint, please include the LOT and REF.
1.3

Adverse incident reporting requirement

All serious adverse events occurring in connection with the product must be reported to Gebrüder Martin
and the respective authorities without delay.
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