Anzeige der Verwendung von bestimmten Biozidprodukten Entgegennahme
Inhalt
<div lang="en-x-mtfrom-de">Notification of the use of certain biocidal products Receipt</div>
Begriffe im Kontext
<div lang="en-x-mtfrom-de">Hazardous Substances Ordinance</div> (Synonym), <div lang="en-x-mtfrom-de">biocidal products</div> (Synonym), <div lang="en-x-mtfrom-de">Biocidal products</div> (Synonym), <div lang="en-x-mtfrom-de">hazardous materials</div> (Synonym)
Fachlich freigegeben am
04.04.2023
Fachlich freigegeben durch
nicht vorhanden
If you use certain biocidal products classified as particularly dangerous in your professional activities, you must notify the competent authority. You must notify the use of biocidal products if you are using biocidal products for the first time or if you are using them again after a break of more than one year.
Declare the use of biocidal products if you use biocidal products in your establishment that
Also report the use of biocidal products if the use category ‘trained professional user’ has been established for them within the framework of the authorisation.
Declare the use of biocidal products if you use biocidal products in your establishment that
- as acute toxic cat. 1, 2 or 3,
- carcinogenic, germ cell mutagenic or reproductive toxicant Cat. 1A or 1B or
- are classified as specific target organ toxicant cat. 1 SE.
Also report the use of biocidal products if the use category ‘trained professional user’ has been established for them within the framework of the authorisation.
- Copy of identification document
- Copy of the certificate(s) of expertise or other relevant qualifications in accordance with Annex I, Section 4.4 (2) of the Hazardous Substances Ordinance - GefStoffV of all competent persons
- If the certificates of competence are older than 6 years: copies of the certificates of participation in the most recently attended training events of all competent persons
They have the relevant expertise for the biocidal product in question. The expertise requirements depend on the type of product, the applications for which the biocidal product is approved and the potential risk to humans and the environment.
Submit the notification in writing or electronically to the responsible authority together with the required documents. The responsible authority will examine your notification. If necessary, it will request further information or documents from you. You will not normally receive a notification confirmation. If you do not meet the requirements, the responsible authority will ask you to correct the deficiencies.
You have fulfilled your reporting obligation if the report is received by the responsible authority on time. As a rule, you will not receive confirmation.
For biocidal products that could be used without expertise under the old version of the Ordinance on Hazardous Substances and that require expertise under the new version of the Ordinance on Hazardous Substances, the expertise requirement under Section 25 of the Ordinance on Hazardous Substances will only apply from 28 July 2025.
This regulation also applies to the use of pesticides which, due to the exception in Annex I No. 3.1 of the old version of the Ordinance on Hazardous Substances (GefStoffV) (use in one's own company), could previously be used without specialist knowledge and which now require specialist knowledge under the new version of the Ordinance on Hazardous Substances.
This regulation also applies to the use of pesticides which, due to the exception in Annex I No. 3.1 of the old version of the Ordinance on Hazardous Substances (GefStoffV) (use in one's own company), could previously be used without specialist knowledge and which now require specialist knowledge under the new version of the Ordinance on Hazardous Substances.
- Notification of the use of particularly dangerous biocidal products is required.
- Display upon first use or after interruption of more than one year.
- Notification when using biocidal products in the company that are classified as:
- acute toxic category 1, 2 or 3,
- carcinogenic, germ cell mutagenic or reproductive toxicant category 1A or 1B,
- specific target organ toxicant category 1 SE.
- Notification also required if use category “trained professional user” has been specified.