Showing results: 1 - 15 of 204 items found.
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ND-2200 -
NDS Products, Inc.
*Three Ranges 0-1000, 0-100, 0-10 mR/hr or 0-10,000, 0-1000, 0-100 uSv/hr*Rugged Dustproof Radiographic Survey Meter
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Radiometrics Midwest Corporation
Radiometrics personnel will come to you and perform site surveys to help in the mitigation of interference or to determine if the environment contains any sources that may interfere with an individuals implanted device such as pacemakers, defibrillators, nerve stimulators, etc.
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Arrow Tech
Measures alpha, beta, gamma, and x-rays. Its digital display shows readings in your choice of counts per minute (CPM), CPS, Sv/hr, or mR/hr, or in accumulated counts. Now with the USB and the Observer USB Software, you can download your accumulated data form the Digilert200's internal memory, set computer alarms, and calibrate your instrument.
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Li-Cor Environmental, Inc.
Pair the Smart Chamber with a gas analyzer of your choosing and connect using your mobile device or laptop via the built-in Wi-Fi web server. See live flux data with a LI-COR gas analyzer or connect to a third-party analyzer and the chamber will log GPS and ancillary data for your flux measurements.
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Keystone Compliance
An EMI site survey is an independent assessment of the potential Electromagnetic Interference (EMI) risks that might interfere with an implantable electrical device such as a pacemaker or defibrillator. The assessment should be completed by a qualified and accredited independent test lab such as Keystone Compliance and in collaboration with the employer, manufacturer of the device, patient and physician. A site survey is conducted by taking various electromagnetic measurements throughout the facility. Keystone Compliance uses a broad range of industry-accepted standards and specifications to determine which electromagnetic fields exist. Following completion of the on-site survey, Keystone Compliance provides the customers with a detailed site survey report that will help identify EMI sources and zones with the potential to interact with an implantable electrical device. This information should then be shared with the physician and employer to develop an action plan to reduce potential negative effects to the patient’s health.