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Direct part marking (DPM) is a process to permanently mark parts with product information including serial numbers, part numbers, date codes, and barcodes. This is done to allow the tracking of parts through the full life cycle. The interpretation of 'permanent' often depends on the context the part is used.
System Center Data Protection Manager (DPM) is a software product from Microsoft that provides near-continuous data protection and data recovery in a Microsoft Windows environment. It is part of the Microsoft System Center family of products and is Microsoft's first entry into the near-continuous backup and data recovery.
Data Position Measurement (DPM) detects these little physical differences to efficiently protect against duplicates. DPM was first used publicly in 1996 by Link Data Security's CD-Cops. SecuROM 4 and later uses this protection method, as do Nintendo optical discs. [citation needed]
Haven is a free and open-source security application for Android designed to monitor activity occurring in the vicinity of a device using its built-in sensors, and to alert the device owner of such activity.
DPM. a variant of the Soviet Degtyaryov machine gun; Detroit People Mover, an automated people mover system; Democratic Party of Macedonians (Demokratska partija Makedonaca), a political party in Serbia; Disappearing Positive Methodology, in the McLaren Report; Direct part marking, permanently marking parts with product information
First YubiKey USB token of the FIDO standard in 2014. The YubiKey is a hardware authentication device manufactured by Yubico to protect access to computers, networks, and online services that supports one-time passwords (OTP), public-key cryptography, authentication, and the Universal 2nd Factor (U2F) and FIDO2 protocols [1] developed by the FIDO Alliance.
DeviceNet is a network protocol used in the automation industry to interconnect control devices for data exchange. It utilizes the Common Industrial Protocol over a Controller Area Network media layer and defines an application layer to cover a range of device profiles.
The Unique Device Identification (UDI) System is intended to assign a unique identifier to medical devices within the United States, Europe, China, South Korea, Saudi Arabia and Taiwan. [1] It was signed into law in the US on September 27, 2007, as part of the Food and Drug Administration Amendments Act (Section 226) of 2007.