PPE, short for “2016/425/EU Personal Protective Equipment,” refers to equipment designed to protect individuals from specific risks in workplaces.
The 2016/425/EU Personal Protective Equipment Regulation covers all equipment designed to protect users from specific hazards. Examples include:
However, certain items, such as dishwashing gloves designed for specific purposes, are excluded from this regulation.
At SERTİFİKE, we provide comprehensive consultancy services to determine the category of PPE products and ensure compliance with regulatory requirements.
SERTİFİKE assists you in meeting CE marking requirements, ensuring your products are both legally and commercially ready.
The CE mark on PPE products signifies that the item complies with relevant regulations and standards. It ensures that the product has been evaluated and deemed safe for human health and the environment.
PPE products are categorized based on the complexity of the risks they protect against:
Category III products, in particular, require a Type Examination Certificate (Module B) along with additional documents evaluating the production processes, such as Module C2 or Module D.
SERTİFİKE offers expert support in managing module-based processes and preparing necessary documentation.
Only notified bodies authorized by the European Union and possessing a 4-digit identification number can issue CE certificates under the PPE regulation. Certificates from unauthorized bodies are considered invalid.
At SERTİFİKE, we collaborate with trusted and authorized notified bodies to complete the certification process for your products securely and reliably.
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