Establishment registration
EUROLATEX SDN BHD
FDA establishment registration 3010599708 · Kedah, MY
Key facts
| Registration number | 3010599708 |
|---|---|
| Establishment name | EUROLATEX SDN BHD |
| Owner/operator | EUROLATEX SDN BHD |
| Owner/operator number | 10084503 |
| FEI number | 3010599708 |
| Address | Plot 33, Kuala Ketil Industrial Estate |
| City | Kedah |
| Country | MY |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | HIS |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 UDI devices (GUDID)
- Current Registration current
- 1–9 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