Commission Implementing Decision (EU) 2021/2148 of 3 December 2021 on the unresolved objections regarding terms and conditions of the authorisation of the biocidal product family Oxybio in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8690) (Text with EEA relevance)

Implementing Decision (EU) 2021/2148 · Decision · 3 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

This Decision applies to the products covered by meta SPC 1 (Oxybio L12) of the biocidal product family identified by the case number BC-SK041671-32 in the Register for Biocidal Products.

Article 2

For the purpose of Article 19(1), point (d), of Regulation (EU) No 528/2012, the hazard classification with regard to the oxidising liquids property of the products referred to in Article 1, shall be Oxidising liquid, Packing group III, in accordance with the UN RTDG Model Regulations, corresponding to Oxidising liquid, Category 3, in accordance with Regulation (EC) No 1272/2008. The products referred to in Article 1 meet the condition laid down in Article 19(1), point (d), of Regulation (EU) No 528/2012 provided that they are classified as Oxidising liquid, Packing group III, in accordance with the UN RTDG Model Regulations, corresponding to Oxidising liquid, Category 3, in accordance with Regulation (EC) No 1272/2008.

Article 3

This Decision is addressed to the Member States.

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

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