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Tags may either be read-only, having a factory-assigned serial number that is used as a key into a database, or may be read/write, where object-specific data can be written into the tag by the system user. Field programmable tags may be write-once, read-multiple; "blank" tags may be written with an electronic product code by the user.
Radar beacon (short: racon) is – according to article 1.103 of the International Telecommunication Union's (ITU) ITU Radio Regulations (RR) [1] – defined as "A transmitter-receiver associated with a fixed navigational mark which, when triggered by a radar, automatically returns a distinctive signal which can appear on the display of the ...
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 ...
June 24, 2024 at 5:10 PM. OMAHA, Neb. (AP) — A new federal rule finalized Monday aims to ensure first responders can find out what hazardous chemicals are on a train almost immediately after a ...
When data are encoded, the characters are translated into machine-readable code. A label or tag containing the encoded data is attached to the item that is to be identified. Machine reader or scanner. This device reads the encoded data, converting them to an alternative form, typically an electrical analog signal. Data decoder.
List of file signatures. This is a list of file signatures, data used to identify or verify the content of a file. Such signatures are also known as magic numbers or Magic Bytes. Many file formats are not intended to be read as text. If such a file is accidentally viewed as a text file, its contents will be unintelligible.
Global Medical Device Nomenclature ( GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
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. The CDRH also oversees the radiation safety performance of non-medical ...