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  1. Microscan
4 December 2017

Microscan Announces New LVS-9585 Verifier for Printed Labels and Direct Part Marks

Microscan, a global manufacturer of barcode readers, verifiers, and machine vision inspection systems for traceability and quality control in industrial manufacturing, announces that it has released the LVS-9585 Handheld Portable Barcode Verifier, providing verification of both printed labels and direct part marks (DPM).

1D and 2D direct part marks are created using methods such as laser etching, chemical etching, and dot peen marking on a variety of surfaces, including metals, plastics, ceramics, and composite materials. They provide a rugged and permanent mark that enables product identification in applications ranging from medical devices to electronic components, as well as automotive, aerospace, and military hardware. To ensure that a part can be accurately and consistently read with a barcode scanner over its operating life, it is critical that the initially applied mark meets minimum readability requirements.

The new LVS-9585 verifies the readability, quality, and data integrity of 1D and 2D printed labels and direct part marks to internationally accepted standards including GS1, ISO 15415/15416, ISO/IEC 29158 TR, and MIL-STD-130N. Microscan’s GS1 certification provides the assurance that the LVS-95XX-series verifiers can help users comply with the U.S. FDA’s Unique Device Identification (UDI) requirements for medical device labels.

The powerful PC-based analysis software allows users to see important pass/fail data and to identify potential problems before they compromise reliable identification of product barcodes. The large field of view allows verification of larger marks. A mounting stand accessory allows large parts with direct part marks to be positioned efficiently for fast verification.

For Direct Part Mark (DPM) applications, the software automatically finds the symbol, cycles through red dome, white dome, and 30-degree angle lighting, selecting the optimal lighting for the material substrate and marking method that are used. The user can then select the optimal lighting for a given part, further optimizing the verification process.

Printed reports and a verification testing data archive featuring both .csv data export and a SQL database interface provide data integration with a user’s quality monitoring system.

Direct marking is an important component of the FDA Unique Device Identification (UDI) regulation. The purpose of UDI is to establish a standard method for...
Meeting compliance requirements for the FDA Unique Device Identification (UDI) rule is priority-one for today's medical device manufacturers and labellers.
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