ISO 13485 – Why should suppliers have a certified Quality Management System (QMS)? ISO 13485 is an international standard that specifies requirements for a quality management system (QMS) for the design, development, production, installation, and servicing of medical devices. It is published by the International Organization for Standardization (ISO). The purpose of ISO 13485 is…
A cleanroom is a room or space designed and built to be free of contamination and airborne particles.
Clamps come in various styles for many different medical purposes and functions.
Radiofrequency (RF) welding is the process of applying alternating electric fields to dipole thermoplastic materials, which results in the generation of heat that melts the sheets together to form a seal.
The medical device industry is continually changing and OEMs need to stay ahead of emerging trends to remain relevant.
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