Certificates
Our certificates prove our compliance with the highest quality and safety standards. They guarantee tested products and processes in accordance with national and international standards.
Decontamination certificate
A decontamination certificate confirms that products have been properly cleaned and disinfected. It is important for hygiene, safety and compliance with legal requirements in sensitive areas.
Note on the German Packaging Act
The German Packaging Act regulates the proper disposal and recycling of packaging. Companies are obliged to register their packaging with a dual system in order to minimise environmental pollution.
Usage-symbols
Best before
Contains latex
Contains DEHP
Lot number
The reuse of this single use medical device might lead to increased risk for the patient and the user; the degree of risk is determined by device and use factors.
This single use medical devices typically have not been designed to be effectively cleaned, decontaminated, allow for removal of reprocessing chemicals do to narrow space between assembled parts or, complex structures
Usage beyond the design intent of the single use device may result in unpredictable loss of functionality: reduced accuracy, reduced performance, altered material, chemical mechanical, biocompatibility properties, impaired compatibility with other devices. Further information please refer:
EUCOMED INDUSTRY GUIDE GUIDE FOR MANUFACTURERS TO IMPLEMENT THE REQUIREMENT INTRODUCED BY DIRECTIVE 2007/47/EC FOR INFORMATION ON SINGLE USE MEDICAL DEVICES
Single use only
This single use medical devices typically have not been designed to be effectively cleaned, decontaminated, allow for removal of reprocessing chemicals do to narrow space between assembled parts or, complex structures
Usage beyond the design intent of the single use device may result in unpredictable loss of functionality: reduced accuracy, reduced performance, altered material, chemical mechanical, biocompatibility properties, impaired compatibility with other devices. Further information please refer:
EUCOMED INDUSTRY GUIDE GUIDE FOR MANUFACTURERS TO IMPLEMENT THE REQUIREMENT INTRODUCED BY DIRECTIVE 2007/47/EC FOR INFORMATION ON SINGLE USE MEDICAL DEVICES
Single use only
Order number
Protect against solar radiation
Refer instruction for use, further information available inside or refer homepage: www.forestadent.com
Product inside is not in sterile condition
Max. /Min. storage temperature
Reprocessing instructions
A reprocessing instruction describes the steps for cleaning, disinfecting and sterilising medical devices. It ensures safety, hygiene and compliance with legal requirements.
Analysis of materials
A bill of materials contains an overview of all materials used in a product. It is used for quality assurance and traceability and helps to evaluate material properties and possible uses.
Safety data sheets
Safety data sheets contain important information about chemical products, including composition, hazards, safe handling and emergency response procedures. They are essential for protecting users and the environment.