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Medical Grade Assistive Technology
AbleNet's ableSAFE assistive technology complies with Europe's Medical Device Regulation (MDR) requirements and is listed with the Food and Drug Administration (FDA) in the United States. AbleNet's rigorous testing protocols, manufacturing quality standards, and proprietary processes are what make AbleNet assistive technology ableSAFE.
ableCARE program removes stress and barriers in implementing AbleNet assistive technology. The ableCARE Product Success team is an extension of your school or clinic team and is standing by ready to provide guidance and knowledge so you and your team build confidence in implementing the AbleNet assistive technology you have invested in. The combination of people and technology enable AbleNet to be actionable now and provide you the resources you need to achieve best outcomes.
ableCARE includes:
Certified third-party laboratories test ableSAFE products to ensure they meet or exceed current global safety standards. When you see the ableSAFE badge, you know you are using a device engineered with safety in mind, made from high-quality materials, and safe for all users.
Some of the regulations and directives tested to include:
ableSTRONG products are designed to be dropped, encounter moisture and dirt, and keep performing so users can achieve best outcomes. Before being approved as ableSTRONG, AbleNet products go through a series of durability tests to ensure they can stand up to a variety of environmental factors.
During the durability testing, AbleNet products must continue working after:
Tested to Meet or Exceed Global Safety Standards
When you see the ableSAFE badge, you know independent third-party laboratories and highly-trained engineers have thoroughly tested the assistive technology. AbleNet designs ableSAFE assistive technology with safety as a priority, rigorously tests each product, and ensures it meets or exceeds the global safety standards of today.
Medical Grade Assistive Technology
AbleNet's ableSAFE assistive technology complies with Europe's Medical Device Regulation (MDR) requirements and is listed with the Food and Drug Administration (FDA) in the United States. AbleNet's rigorous testing protocols, manufacturing quality standards, and proprietary processes are what make AbleNet assistive technology ableSAFE.
Designed With Safety in Mind
ableSAFE is more than a badge; it's a level of quality you should expect from all assistive technology. AbleNet relieves the stress of worrying about product safety by rigorously testing ableSAFE assistive technology to ensure it meets or exceeds the global safety standards of today. Safety is a top priority during the design process of AbleNet's ableSAFE assistive technology. Using materials free of lead and phthalates, removing sharp corners and edges, and ensuring electronic designs do not create a risk of electrical shock are some of the precautions taken during the design process.
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Scarborough, Ontario M1S 3Y6
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