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Hi
I have several "accessories" used to color devices that are classified as part of a "generic device group".
The accessories and generic device group fall under the MDD (until 2024) and are classified as Class IIa.
We would like to market many of the accessories as a "demo set".
Each of the accessories in the "demo set" are individually labeled with the CE and the other standard information and each is listed on the Declaration of Conformity for the brand.
Does the name of the liquid Demo Set (kit) need to be listed on the "Declaration of Conformity" for the brand?
Thanks