Medical devices demand digital traceability.

Veribl provides a digital layer for medical devices that connects manufacturers to every device in the field. A QR code on each device links to registration, digital IFU, warranty status, service history, and safety communications. This improves UDI compliance, enables faster recalls, reduces IFU-related complaints, and provides post-market surveillance data — all from a single platform.

Yes. Veribl's serialized QR codes can encode or link to UDI data including Device Identifier (DI) and Production Identifier (PI). Each device's digital record maintains its full identification chain — manufacturer, model, lot/batch, serial number, and expiration date. This supports both FDA UDI and EU MDR requirements for device traceability.

When a recall is issued, Veribl identifies all registered devices matching the affected criteria (lot, serial range, date range) and sends direct notifications to registered owners or facilities. You get real-time tracking of recall acknowledgment rates, can send automated follow-ups to non-respondents, and maintain a complete audit trail for regulatory reporting.

Veribl can supplement or replace paper IFU with digital versions accessible via QR scan. Digital IFU can be updated instantly when documentation changes — no reprinting or redistribution required. This is particularly valuable for devices with frequent software updates or revised protocols. Note: check local regulations as some markets still require paper IFU availability.

Each device's digital record tracks its complete service history — calibrations, preventive maintenance, parts replacements, and field corrections. Automated alerts notify device owners when calibration or maintenance is due. Your service team can verify the full history before any intervention, and you maintain audit-ready records for regulatory inspections.

Yes. Veribl works across Class I, II, and III devices. The platform's flexibility allows configuration for different documentation requirements, warranty terms, and service schedules per device class. For Class III devices with more stringent post-market surveillance requirements, Veribl's data capture capabilities provide the real-world evidence regulators expect.