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InterTech Development Company UDI System Announced
Date:4/19/2010

Medical device manufacturers seeking to comply with the FDA Amendments Act of 2007 and to enhance patient safety with complete part traceability, can now use the InterTech Development (www.intertechdevelopment.com) Unique Device Identifier (UDI) System, which integrates bar coding, scan and software tracking of each part and batch, including all leak test, functional test and lifecycle test data related to each component

(Vocus) -- Medical device manufacturers seeking to comply with the FDA Amendments Act of 2007 and to enhance patient safety with complete part traceability, can now use the InterTech Development (www.intertechdevelopment.com) Unique Device Identifier (UDI) System, which integrates bar coding, scan and software tracking of each part and batch, including all leak test, functional test and lifecycle test data related to each component (http://www.intertechdevelopment.com/instrumentation_detail.cgi?id_num=143 ).

The InterTech Development UDI System not only provides full traceability in the event of product recalls, but also provides data for process optimization to streamline production, and storage of all test data at each productions stage for SPC (Statistical Process Control) data that underlies most quality assurance systems and full ISO 13485:2003 compliance.

For added traceability, a laser marking system can be integrated with the bar code label system.

Jacques Hoffmann, President of InterTech Development Company, comments, “InterTech’s turnkey test solutions have always emphasized software integration to
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Source: PRWeb
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