The IVDR, in force since May 26, 2022, represents a turning point in the EU-wide harmonization of patient safety. At the same time, it places high demands on us as manufacturers and on you as a user of in vitro diagnostic medical devices to implement the new regulation. We would like to meet this challenge together with you for the benefit of your patients. It is important to us to certify our portfolio of diagnostic solutions in compliance with the IVDR in due time. Therefore, we would like to keep you informed about our progress with the implementation of the IVDR.
Currently, we do not have the capacity to produce customized antibodies. We are happy to put you in touch with reliable partners. You can contact us via phone +49 30 804 984 990 or via mail to firstname.lastname@example.org.
IThe technical datasheet of every antibody lists the tested reactivity of the antibody. This does not mean that the antibody does not react with species not listed, but that they have not been verified. If the desired reactivity of the antibody is not listed, please contact us via phone +49 30 804 984 990 or via mail to email@example.com. We are happy to check if the antibody is suitable for your application.
Delivery is on account and at the costs of the purchaser.
The delivery time for our products is about 5 to 15 days.
A mercury-vapor lamp (100 Watt) is optimally suited for FISH.