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Regulation (EC) No 2037/2000 ANNEX I

Regulation (EC) No 2037/2000 ANNEX I

ANNEX ISupplementary provisions

ANNEX I Pursuant to paragraph 3 of Decision XII/2 of the 12th Meeting of the Parties to the Montreal Protocol on measures to facilitate the transition to chlorofluorocarbon-free metered-dose inhalers (MDIs), the following Parties have determined that, due to the presence of suitable non-CFC MDIs, CFCs no longer qualify as ‘essential’ under the Protocol when combined with following products: Product Country Salbutamol Terbutaline Fenoterol Orciprenaline Reproterol Carbuterol Hexoprenaline Pirbuterol Clenbuterol Bitolterol Procaterol Beclomethasone Dexamethasone Fluinisolide Fluiticasone Budesonide Triamcinolone Ipratropium bromide Oxitropium Bromide Austria X X X X X X X X X X X                 Belgium X X X X X X X X X X X                 Czech Republic X X X X X X X X X X X                 Denmark X X X X X X X X X X X                 Finland X                                     France X                                     Germany X X X X X X X X X X X X X X X X X X X Greece X X X X X X X X X X X                 Ireland X                                     Luxembourg X                                     Portugal X X X X X X X X X X X                 The Netherlands X X X X X X X X X X X                 Norway X X X X X X X X X X X                 Sweden X                                     UK X                                     Source: www.unep.org/ozone/dec12-2-3.pdf

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Other provisions in Regulation (EC) No 2037/2000

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

CitationANNEX I of Regulation (EC) No 2037/2000 (LawPlayer, data as of 2026-07-04)

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