ISO 13485 is designed for use throughout the life cycle of a medical device. It supports each stage of medical device development and operation from initial concept to production and disposal. The standard helps internal and external parties certify and validate processes which maintain the stability of quality management systems (QMS).
Electrical & Device Mfg.
Dual Wire ESD Monitors and Wrist Straps – vs Single Wire – What’s the Difference? Reposted from Our Friends at SCS-Static-Control Solutions Dual wire ESD
Overall size and method of attachment is crucial to ideal fit and function. Off-the-shelf solutions don’t always fit specific requirements for outdated or rare hardware. Custom designed IC sockets accommodate rare device configurations, odd sizes, and alternate mounting configurations.
We ran into this fantastic soldering demo on YouTube using PACE equipment. View Production Automation’s YouTube Channel View all the PACE products Production Automation offers
Dry Box Desiccant Storage within the PCB Manufacturing Environment: Uses, History, Selection, and Performance
Manufacturing Uses of Desiccator Cabinets for Printed Circuit Boards (PCBs) The discussion regarding ‘dry box’ or desiccant storage of MSD’s (Moisture Sensitive Devices) has increased