Establishment registration
MAXWELL GLOVE MANUFACTURING BHD
FDA establishment registration 3004939660 · KAMUNTING Perak, MY
Key facts
| Registration number | 3004939660 |
|---|---|
| Establishment name | MAXWELL GLOVE MANUFACTURING BHD |
| Owner/operator | MAXWELL GLOVE MANUFACTURING BHD |
| Owner/operator number | 9010439 |
| FEI number | 3004939660 |
| Address | PLOT 116 & 117, JALAN LOGAM 7, KAWASAN PERINDUSTRIAN KAMUNTING RAYA 3. |
| City | KAMUNTING Perak |
| Country | MY |
| Registration valid through | 2026 |
| Product codes listed | LYY, LZA |
| Device classes | 1 |
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