Resource Centre
Discover a wealth of knowledge and insights from the experts at StarFish Medical. Our Resource Centre offers product development tips, reviews of new and cutting-edge technologies, and in-depth articles on regulatory updates and compliance in medical device development.
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The main success criteria for medical device companies after earning FDA regulatory clearance is securing positive coverage decisions from payers. While regulatory approval is sufficient to get a product to market, it has no bearing on product adoption. The availability of reimbursement has a direct impact on therapy adoption – it can “make or break” a product1. This primer provides an overview of US reimbursement codes and when they are used to help determine coverage and payment for medical devices.
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When COVID is Under Control – StarFish Medical employee choices for their first activities when COVID restrictions are eased.
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Designing BLDC motor drive electronics focuses on the particular strategy of driving the motor windings with sinusoidal waveforms.
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FDA Approved or Cleared Medical Device – the pathway you choose depends on the level of risk it represents and its intended use.
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3D Printed Parts Streamline Development provides context for designers using 3D printed parts as a part of their market-ready medical devices.
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Mechanical Engineering Team lead shares his response to students who ask him what the ideal medtech co-op looks like.
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Medical Device Camera Sensor technical trade-offs to consider when incorporating a visible or near-infrared range camera sensor into a medical device.
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Optical Safety for Ophthalmic Instruments covers safety limits and maximum exposure limits of wavelengths in the IR, UV and visible light spectrum.
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Maximize medical device optical signals by keeping sensor and control signals correlated and other strategies are discussed in this article.
