Not regulatory advice.
Last updated: 2026-05-24
What MedevIQ is
MedevIQ is a medical-device reference layer. It reconciles device identity, manufacturer information, regulatory pathway, adverse-event signals, and recall history from authoritative public sources (CDSCO, FDA, EUDAMED, Health Canada, TGA, PMDA, MHRA, NMPA) and presents them in a single queryable record per device and manufacturer.
What MedevIQ is not
MedevIQ is not a regulatory submission tool, clinical decision-support system, procurement contract, or substitute for professional regulatory judgement. Records are sourced and dated but may lag the latest regulator action by the refresh cadences listed on the Status page.
For regulatory use
Always confirm regulatory status, classification, and current recall posture with the relevant regulator directly before making a submission, marketing, import, or procurement decision. The presence or absence of a record in MedevIQ does not constitute the official regulatory position.
For procurement use
Hospital and procurement teams should treat MedevIQ as one input alongside the regulator's authoritative database, the manufacturer's representations, and your own technical and clinical assessment. We provide source attribution on every record so you can verify.
Reporting issues
If a record on MedevIQ contains an error that could affect a regulatory or procurement decision, email [email protected] with the record identifier and the discrepancy. We respond within 5 business days.