Reed Tech offers medical device data management and submission solutions for multiple regulatory authorities’ Unique Device Identifier Databases. We are a leading provider of Structured Product Labeling preparation and submission services. We apply a decade of experience to help device manufacturers fulfill UDI submission requirements.
The Reed Tech solution accepts data from manufacturers’ existing repositories, verifies per FDA’s specifications, builds and submits SPL data messages, and processes acknowledgement messages – all in a secure and compliant environment. Our solution provides timely, accurate submission and maintenance of GUDID records and will support future global UDID submissions.