This site uses modern web standards that aren't supported by your browser. For best results, please upgrade to Google Chrome, Microsoft Edge, or Mozilla Firefox.

Reed Tech SingleSource™ for Medical Devices

Reed Tech SingleSource™ for Medical Devices

Medical Device Product Data Management & Syndication

Reed Tech SingleSource™ was built just to meet the product data needs of Medical Device manufacturers.

Central Product Data Management

Store product data in a secure cloud repository

Simple Data Syndication

Share your latest data with downstream users anywhere

Traceability & Control

View audit trails and version history with simple reports

Compliance & Security

Meet 21 CFR Part 11 requirements in a fully verified system

Expert Support

Get help when you need it

EU Medical Device Regulation (MDR) UDI Submission

Confidently and efficiently distribute accurate product UDI data to EU MDR and (future) multiple regulatory agencies and commercial partners throughout the world, each with different regional requirements, or integrate with existing PIM/MDM systems and provide the “last mile” support

FDA Class I

Class I Devices, and devices that have not been classified into class I, class II or class III that are required to be labeled with a UDI, must bear UDI as a permanent marking on the device itself if the device is one that is intended to be used more than once and intended to be reprocessed before each use. §801.45. The compliance date is September 24, 2020.

EU UDI

The (EU) Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), originally published in 2017 by the EU Parliament, sets forth new regulatory requirements for medical device and in vitro diagnostic device manufacturers that distribute products in the EU. To comply with the new requirements, manufacturers will need to submit MDR certifications and device registration in EUDAMED by May 26, 2020.

Day(s)

:

Hour(s)

:

Minute(s)

:

Second(s)

Day(s)

:

Hour(s)

:

Minute(s)

:

Second(s)

Reed Tech SingleSource and GDSN Syndication with 1WorldSync

Full Lifecycle Control

Device Specific Dataset

Focus your data collection efforts on industry-specific fields.

Simple Dashboard Management

See the state of all your data records at a glance

Easy record syndication

Publish the right data for the right audience in just a few clicks

Integrated GDSN Syndication

Share your data with downstream users

NHS eProcurement

Meet the National Health Service eProcurement requirements

Hospital Networks

Allow providers easy access to your devices

GPOs and Major Buyers

Give buyers all the information they need to purchase

Global Roadmap

Know you can meet new demands as they arise

Access to the Global Data Synchronization Network

GDSN publishing through 1WorldSync™, the leading provider of product content solutions

NHS eProcurement Requirements Webinar

Request a Preview

Please provide the following information to connect with a representative

Featured Resources

EU MDR-5 Things to Know for Pre-Planning

Medical Device Unique Device Identification Challenges and Solutions

How to Efficiently Share Medical Device Product Data through GDSN

By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close