Intertek is a leading provider of compliance, certification, consulting,
and testing services for medical electronics manufacturers and brand
owners. The scope of many environmental regulations either currently
includes, or is expected soon to add medical devices.
Intertek’s environmental compliance services for medical products, their
packaging, and their accessories span the full range of global requirements
including EU RoHS, EU WEEE, California Proposition 65, REACH, China RoHS,
Korea RoHS, Japan Green, EU Packaging Directive, EU Battery Directive,
IEC 60601-1-9, Health Canada mandated testing for Di (2-ethylhexyl)
phthalate (DEHP) and Bisphenol-A (BPA), and evolving global requirements.
“…After carefully studying the petition and the oral and written
comments, we are not convinced that all of these medical device
products require special regulations that treat them differently than
other products falling within the jurisdiction of Proposition 65.”
- Office of Environmental Health Hazard Assessment –
Government of California
Intertek has a comprehensive suite of services for restricted materials,
recycling, product testing, product declaration (including materials
declarations and treatment instructions), recycling registration, packaging
requirements, implementation of recycling systems, product labeling, and
consulting.
Sample of Intertek’s Restricted Substances and Recycling Services
>> For other services or for more information,
click here.
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