Medical Device Safety Services Available In Australasia
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based in GERMANY
When it comes to medical devices, quality and safety are especially vital. As a notified body, we can help you with your conformity assessment procedure and ensure that your active and non-active medical devices comply with EU Directive 93/42/EEC. Tap into the European ...
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based in USA
Our skilled engineering team excels in low-level programming for embedded systems, enabling high-performance applications on diverse hardware. We adhere to top industry standards for connectivity, reliability, and performance. Plus, we provide firmware development for multiple architectures like ARM, RISC-V, x86, and ...
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by STEMartbased in USA
/EC, which outline the safety and performance requirements for active medical electrical equipment, non-active medical devices, and in vitro diagnostic medical devices. In order to place a medical device on the European market, manufacturer must obtain a CE mark. ...
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based in USA
In the medical field, practitioners utilize a range of devices to address patient health, from diagnosis to surgery. When the patient comes into contact with a medical device or material, it should fulfill its intended function without harming the patient. Therefore, all medical devices need to ...
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