Commission Implementing Decision (EU) 2021/1315 of 6 August 2021 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 Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 5821) (Only the Polish text is authentic)
Information
Type
Implementing decision
Regulated products
Medical Devices
Published
August 6, 2021
Last updated
August 6, 2021
Description
Commission Implementing Decision (EU) 2021/1315 extends the use of biocidal product Biobor JF in Poland under Regulation (EU) No 528/2012.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0