DeviceOS guided demo
See DeviceOS in action
The bundle view: QualityOS and RegulatoryOS on one record set, one identity and one audit trail.
Illustrative screens with sample data — no sign-up, nothing to install, and no real customer records. Share this link with anyone.
Step 1 of 4
One device record
Product families, models, UDI-DI and classifications resolve to a single device record every module reads from.
DeviceOS / Devices / Pedicle screw system
Device record — TITAN-PS
Identification
- UDI-DI: 00889999123456 (auto-pulled from AccessGUDID)
- Catalog: PS-4525 through PS-6580
- Classification: US Class II / EU Class IIb
Linked records
- Design history file: DHF-014
- Risk file: RMF-014 (ISO 14971)
- Registrations: 4 markets
- Open quality records: 3
What makes DeviceOS different
The parts a generic document system or spreadsheet cannot do
One device record, every discipline
Quality, regulatory and evidence modules read the same product record — UDI-DI, model, class and market status — so nothing is re-keyed between teams.
Automatic UDI enrichment
Enter a company and part number and the record pulls its GUDID attributes from the FDA AccessGUDID database automatically.
Portfolio-level clocks
Registrations, PMS reporting periods and post-market data obligations roll up per device family rather than per spreadsheet tab.
Bundled economics
DeviceOS bundles the quality, regulatory and evidence applications for manufacturers who need all three, at a lower total than buying them separately.
Answers, not a sales call
The ten questions everyone asks about DeviceOS
Answered here in full. Anything else, ask below and you get an immediate answer.
The combined bundle: QualityOS, RegulatoryOS and the supporting modules under one licence, one login and one set of records.
Ready to use DeviceOS with your own records?
Start a subscription, or ask us for a live walkthrough with your device portfolio.