Medical Assembly and Packaging

GDM entered the Medical Assembly and Packaging market in 1989 and was registered by the FDA in 1992 to provide Class I and Class II medical device assembly services.

GDM is ISO 13485:2016 registered and can assist in creating compliant manufacturing processes that include inspection points, material reconciliation, and product validation.

-Medical Devices

-Diagnostic Kits

-Media Kits

-Re-pack, Re-label

-Packaging Validation

-Class 10K Cleanroom

All materials and operations are transacted through our manufacturing software to provide comprehensive batch records and real time completion status.

Compliant assembly and packaging services

GDM Electronic & Medical, LLC - 2020