Dear Customers,
We will be on our Christmas break from 23 December 2025 at 1:00 p.m. and will be available again from 5 January 2026.
Please note that new registrations and requests requiring manual processing will only be handled from this date onwards.
You may, of course, place orders and access downloads online at any time.
We wish you happy holidays, a restful break, and a healthy start to the New Year!
Your DIN Media
Standard [WITHDRAWN]
Product information on this site:
Quick delivery via download or delivery service
All transactions are encrypted
This document is an adaptation to the structure and state of DIN EN 60601-1:2007 with the accompanying supplementary standards. For laser devices, this is a new "state of the art" which is necessary for compliance with the basic requirements of the medical products law. The German version is an identical technical takeover of the IEC version, so that there are no trade restrictions for the worldwide distribution of laser devices. In addition to the medical sector, the standard is also applicable to the cosmetics sector in order to achieve a uniform level of safety. The responsible committee is DKE/K 812 "Elektromedizinische Geräte" ("Electro-medical equipment") of the DKE (German Commission for Electrical, Electronic and Information Technologies) at DIN and VDE.
This document replaces DIN EN 60601-2-22 Berichtigung 1:1997-11; VDE 0750-2-22 Berichtigung 1:1997-11 , DIN EN 60601-2-22:1996-12; VDE 0750-2-22:1996-12 .
This document has been replaced by: DIN EN IEC 60601-2-22:2022-10; VDE 0750-2-22:2022-10 .