{"id":509768,"date":"2024-11-05T14:08:26","date_gmt":"2024-11-05T14:08:26","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/cga-m-20-2017\/"},"modified":"2024-11-05T14:08:26","modified_gmt":"2024-11-05T14:08:26","slug":"cga-m-20-2017","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/cga\/cga-m-20-2017\/","title":{"rendered":"CGA M-20-2017"},"content":{"rendered":"

This publication describes the industry position of both manufacturers and distributors of medical devices used in the medical gas and gas equipment industry regarding 21 CFR Part 830 and associated guidance. It describes the industry's interpretation and application of the requirements for the creation and maintenance of device barcodes and the submission of the related database records in electronic format. This pub-lication should be utilized to create a firm's standard operating procedures (SOP) for compliance with the regulation. <\/p>\n

This publication is based upon: <\/p>\n