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Patent Application Information Retrieval ( PAIR) is an online service provided by the United States Patent and Trademark Office to allow users to see the prosecution histories of United States patents and patent applications and obtain copies of documents filed therein. There are two services: Public PAIR, which allows the general public to ...
Rakon Limited is a technology company founded in 1967 that designs and manufactures frequency control products, primarily quartz crystals and temperature-compensated crystal oscillators ( TCXO ), [1] oven controlled crystal oscillators ( OCXO) and voltage controlled crystal oscillators ( VCXO ). [2] Its head office is in Auckland, New Zealand ...
A Central Equipment Identity Register (CEIR) is a database of mobile equipment identifiers ( IMEI – for networks of GSM standard, MEID – for networks of CDMA standard). Such an identifier is assigned to each SIM slot of the mobile device. Lists of IMEIs may be the: White – for devices that are allowed to register in the cellular network ...
Mario Cardullo's device, patented on January 23, 1973, was the first true ancestor of modern RFID, as it was a passive radio transponder with memory. The initial device was passive, powered by the interrogating signal, and was demonstrated in 1971 to the New York Port Authority and other potential users.
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The Android app was released in January 2010, and for iOS on February 8, 2011, after an HTML5 web application was released for iOS users in August 2008. The Android app is compatible with devices running at least Android 2.1, while the iOS app is compatible with iPod Touches, iPads and iPhones updated to iOS 7.0+.
Related: 'RuPaul's Drag Race All Stars 8' Take New York. Next Stop: the World. In each episode, the queens will compete for Benefactress Badges with the three queens who collect the most badges ...
FDA Laboratory Building 62 (Engineering and Physics) houses the Center for Devices and Radiological Health. The Center for Devices and Radiological Health (CDRH) is the branch of the United States Food and Drug Administration (FDA) responsible for the premarket approval of all medical devices, as well as overseeing the manufacturing, performance and safety of these devices.