Medical Device Manufacturers
Global UDI Compliance Software
Our global UDI solution streamlines submissions to EUDAMED, GUDID, ausUDID and swissdamed and all key global registries. Guarantee data integrity, meet regulatory requirements, and secure market access for your medical devices worldwide.
Why Innovit
Product Data Solutions for the Healthcare Supply Chain
Innovit streamlines regulatory compliance, global commerce, and supply chain efficiency with our integrated suite of UDI, GDSN, PIM, and MDM solutions.
Compliance with Regulatory & Industry Standards
Automate validated & error-free submissions to GUDID, EUDAMED, and other UDI registries worldwide while maintaining full audit-readiness.
Faster Product Launches & Better Operational Efficiency
Speed up time-to-market for new products and eliminate error-prone manual tasks to streamline healthcare procurement, global commerce, and supply chain workflows.
Verified Product Data for Patient Safety & Clinical Care
Improve care outcomes by delivering verified product master data from the manufacturer directly to hospital ERPs and point-of-care systems.
Who We Help
Organizations We Empower
Trusted product data solutions for medical device manufacturers, distributors, GPOs, and healthcare providers.
Distributors & GPOs
Centrally manage product data aggregation and enrichment to streamline contract pricing, procurement workflows, and logistics operations with your trading partner network.
Medical Device Manufacturers
Automate global UDI compliance and streamline the syndication of verified product data to GPOs, distributors, and hospital networks.
Healthcare Providers
Enhance patient safety and clinical outcomes by integrating accurate, real-time product master data into ERP, EHR, EMR, and point-of-care workflows.
570K+ UDI
Over 570,000 records registered on GUDID and EUDAMED.
6.5M PIM & MDM
Largest PIM & MDM sites manage over 6,500,000 master data records.
87% GDSN
Certified by leading GDSN data pools, syncing 87% of global GTINs.
Solutions Overview
Scalable SaaS solutions to navigate complex global regulations, accelerate product launches & drive operational excellence across the healthcare ecosystem.
UDI Compliance
Centralize and automate UDI submissions to global regulatory databases including GUDID, EUDAMED, ausUDID, swissdamed and more, through a validated, audit-ready framework.
Pre-packaged UDI attributes, code lists and validation rules
Comprehensive audit trails and device submission history
Compliant with applicable data management, system validation & security standards
GDSN Data Syndication
Synchronize verified product data with global trading partners through your choice of GDSN data pools like atrify, GHX, Syndigo, and NPC.
Pre-configured GS1 attributes and data validation logic
Full visibility into publication and message exchange history
Certified connectivity to major GDSN data pools
Product Information Management (PIM)
Enrich and optimize product content for diverse sales channels and global markets to drive digital commerce and operational efficiency.
Centralized management of rich product content and digital assets (DAM)
Automated workflows for data quality and localized enrichment
Seamless content syndication across e-commerce and trading partner portals
Master Data Management (MDM)
Establish a trusted “Golden Record” for products, suppliers, and locations to eliminate silos and streamline business-critical processes.
Multi-Domain MDM within a single, intuitive interface
Advanced data stewardship and automated data cleansing tools
Bi-directional synchronization with ERP, PLM, RMS, EHR and other IT systems.
Trusted By
Industry Leaders
We’re proud to work alongside industry-leading healthcare brands that trust us to drive innovation and success.
What Our Customers Say
What Our Customers Say
Meeting FDA GUDID and GDSN Deadlines: A UDI Compliance Success Story
“We were at risk to miss the UDI Class II deadline of September 2016 and our team in Australia suggested Innovit. After an extensive RFP process involving numerous solutions, the path forward was clear.
Within eight months from project kick-off, we were able to submit data to the FDA’s GUDID system, while meeting the GDSN MJR3 May 6th deadline.”
Ready To Get Started?
Partner with Innovit for Faster Time-to-Value
Join leading device manufacturers and healthcare organizations who trust Innovit to manage their most critical product data.
Schedule a discovery session to address your specific UDI compliance, GDSN syndication, or PIM/MDM requirements
Understand how Innovit integrates into your specific IT environment and timelines to ensure rapid time-to-value
Explore our SaaS capabilities through a hands-on trial environment