Establishment registration
DUOJECT MEDICAL SYSTEMS, INC.
FDA establishment registration 9613744 · BROMONT Quebec, CA
Key facts
| Registration number | 9613744 |
|---|---|
| Establishment name | DUOJECT MEDICAL SYSTEMS, INC. |
| Owner/operator | Duoject Medical Systems |
| Owner/operator number | 9038613 |
| FEI number | 3002771638 |
| Address | 50 CHEMIN DE GASPE |
| City | BROMONT Quebec |
| Country | CA |
| Establishment types | Specification developer, Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | LHI |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database