Establishment registration
BeamMed Ltd.
FDA establishment registration 3006701790 · Petah Tikva Central, IL
Key facts
| Registration number | 3006701790 |
|---|---|
| Establishment name | BeamMed Ltd. |
| Owner/operator | BeamMed Ltd |
| Owner/operator number | 10024010 |
| FEI number | 3006701790 |
| Address | 8 Ha-Lapid Street |
| City | Petah Tikva Central |
| Country | IL |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | MUA |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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