Commission Implementing Decision (EU) 2023/2634 of 27 November 2023 concerning the extension of the action taken by the Polish Office for Registration of Medicinal Products, Medical Devices and Biocidal Products permitting the making available on the market and use of the biocidal product Biobor JF in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2023) 7951)
Information
Type
Implementing decision
Regulated products
Medical Devices
Published
November 27, 2023
Last updated
November 27, 2023
Description
Commission extends permission for the use of biocidal product Biobor JF in accordance with EU regulations.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0