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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)

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)

Implementing Decision (EU) 2021/1315 · Decision · 2 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Article 1

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The Polish Office for Registration of Medicinal Products, Medical Devices and Biocidal Products may extend the action to permit the making available on the market for, and use by, professional users of the biocidal product Biobor JF for the preventive and curative antimicrobial treatment of aircraft fuel tanks and fuel systems until 6 November 2022.

Article 2

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This Decision is addressed to the Polish Office for Registration of Medicinal Products, Medical Devices and Biocidal Products. It shall apply from 6 May 2021.

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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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