Innovit Helps Medical Devices Manufacturers Meet Regulatory Compliance, Reduce Counterfeiting with UDI Multi-Connector Product
Retrieved on:
Tuesday, June 12, 2018
SAN FRANCISCO, June 12, 2018 /PRNewswire/ -- Innovit , a global master data management solution provider, today announced the availability of its Unique Device Identification (UDI) Multi-Connector solution, which helps medical device manufacturers keep pace with regulatory compliance standards and reduce the threat of counterfeiting by automating UDI data submissions to a host of regulatory databases.
Key Points:
- SAN FRANCISCO, June 12, 2018 /PRNewswire/ -- Innovit , a global master data management solution provider, today announced the availability of its Unique Device Identification (UDI) Multi-Connector solution, which helps medical device manufacturers keep pace with regulatory compliance standards and reduce the threat of counterfeiting by automating UDI data submissions to a host of regulatory databases.
- Innovit's UDI Multi-Connector helps global medical device manufacturers manage and automate the submission of UDI data using the HL7 SPL data format and messaging protocol required by the FDA and proposed by the EU Commission.
- Innovit also stores a complete message exchange history, which provides organizations with full visibility and traceability of their data submission history.
- Innovit's UDI MultiConnector allows global medical device suppliers to achieve compliance with UDI requirements while reducing operational, SQA and other IT costs.