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The device was tested for 500 voltammetric cycles, maintaining its electroactivity and chromatic contrast.
The LFD device was tested for its specificity, sensitivity and storage stability.
Effectiveness of the method and device was tested for the reference demagnetized magnet dedicated for magnetostrictive actuators.
The DLLME method with the proposed device was tested for the enrichment of glycyrrhizic acid from aqueous extracts of licorice before analysis by a HPLC method.
The performance of this device was tested for the simultaneous detection of the mycotoxins ochratoxin A (OTA), aflatoxin B1 (and1) andeoxynivalenolol (DON) which are strictly regulated food contaminants with severe detrimental effects on human and animal health.
The device was tested for magnetic resonance imaging (MRI) compatibility and found compatible, so that the MRI results would not be affected by the US device.
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After being cycled between two temperatures, say -55C to 125C for 1000 times, a device is tested for its function, and then sectioned and examined in microscopes for failure modes (e.g., distortion and cracking).
BMI, limb circumference and duration of application of the device were tested for inclusion in the mixed model.
Both versions of the device were tested for haemostasis of and tissue grip on renal arteries in six anaesthetised pigs.
A lithium ion cell designed for implantable medical devices was tested for its performance as a power source for left ventricular assist devices (LVAD) or total artificial hearts (TAH).
The devices are tested for both analog and digital circuits.
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