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Art. 15a Unique formula identifier 59
1 If a manufacturer places a preparation on the market which is classified as dangerous because of the physical or health hazards it poses, the manufacturer must label the preparation with a unique formula identifier (UFI). 2 He must generate the UFI using the electronic system provided by the Notification Authority. Generating the UFI using the electronic system is not required if the preparation already has a UFI that has been generated on the basis of the CLP Regulation60. 3 The UFI, preceded by the acronym "UFI:" in capital letters, must be printed or affixed in a clearly visible, legible and indelible manner in the following location:
4 In the case of preparation that are not packaged, the UFI must be indicated on the safety data sheet or, in the case of supply to private users, in a copy of the label elements in accordance with Article 29 paragraph 3 of the CLP Regulation, together with the other label elements. 5 Paragraphs 1–4 do not apply if the preparation is not subject to the obligation to notify in accordance with Article 54. 59 Inserted by No I of the O of 31 Jan. 2018 (AS 2018 801). Amended by Annex No 1 of the O of 18 Nov. 2020, in force since 1 Jan. 2022 (AS 2020 5125). 60 See footnote to Art. 2 para. 4. |