COMMISSION IMPLEMENTING REGULATION (EU) 2025/1138 | 32025R1138 — European Union law | Esheria

COMMISSION IMPLEMENTING REGULATION (EU) 2025/1138

Tevan B.V. is granted a Union authorisation for the biocidal product family ‘Tevan Panox Family’ and may place it on the market and use it only according to the Annex conditions.

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Jurisdiction
European Union
Instrument
Regulation
Citation
32025R1138
Status
In force
Version
Undated source snapshot
Language
en
Official source
View official record ↗
PPE biocidal product use chemical safety disinfectants disinfection disposal food industry occupational safety product authorisation product handling product use conditions product use instructions professional use respiratory protection risk mitigation room re-entry storage storage and disposal surface treatment ventilation veterinary hygiene water system treatment workplace protective equipment

Statute overview

About this statute

Tevan B.V. is granted a Union authorisation for the biocidal product family ‘Tevan Panox Family’ and may place it on the market and use it only according to the Annex conditions. The text sets detailed use conditions for a product, including protective equipment, ventilation, room-size limits, re-entry restrictions, and keeping third parties and animals away from treated areas. Professional users must follow strict handling rules for this product, including PPE, ventilation, room-size limits, and access restrictions. This provision sets use instructions and safety measures for a biocidal disinfectant across several indoor applications, including dilution levels, surface contact time, PPE, ventilation, access limits, and disposal/storage instructions. This provision sets detailed use instructions and safety rules for disinfecting surfaces and water systems with the product, including PPE, ventilation, room access limits, waiting times, and storage conditions.