ANZER Receives OSU Project Award
——-Press Release——- ANZER, a leading provider of electronic contract manufacturing services, announces its collaboration with The Ohio State University. Akron, OH, February 20, 2024 — ANZER, a full-service contract electronic designer and manufacturer, is pleased to announce it has been awarded a contract from The…
Internet of Medical Things (IoMT) Manufacturing Certifications
The certifications required to manufacture Internet of Medical Things (IoMT) devices can vary depending on the specific type of device and the regulations in the target market. However, there are some common certifications and standards that medical manufacturers often need to adhere to. Here are…
PCB Assembly Ionic Contamination: What to Know
Ionic contamination in PCB (Printed Circuit Board) assembly refers to the presence of ionic residues on the surface of the assembled PCB. The chemicals and materials used in manufacturing and assembly typically leave these residues behind. Ionic contamination can harm electronic circuits’ performance and reliability,…
ANZER Completes 2nd Phase of ISO 13485 Medical Certification
——PRESS RELEASE—— Akron, OH, November 22, 2023 – ANZER, a full-service contract electronic design and manufacturer, announces the completion of the second phase of its audit for ISO 13485 medical manufacturing certification. ISO 13485 is an international standard that specifies requirements for a quality management system for…
Q: Electromagnetic Emissions: Harmful or Not
A: Electromagnetic emissions refer to releasing electromagnetic energy through waves or particles. Electromagnetic energy is a fundamental force responsible for many phenomena, including light, radio waves, microwaves, X-rays, and gamma rays. These emissions are produced by moving charged particles, such as electrons, within atoms and…
Q: What is ISO 13485 Medical
A: ISO 13485 Medical is an international standard that specifies requirements for a quality management system for medical devices. It outlines the processes and controls that medical device manufacturers must follow to ensure their products’ safety, reliability, and effectiveness. Compliance with ISO 13485 demonstrates a…