Establishment registration
STERIPACK ASIA SDN BHD
FDA establishment registration 3009988302 · Klang Selangor, MY
Key facts
| Registration number | 3009988302 |
|---|---|
| Establishment name | STERIPACK ASIA SDN BHD |
| Owner/operator | SteriPack Asia Sdn Bhd |
| Owner/operator number | 10043162 |
| FEI number | 3009988302 |
| Address | Lot 119992, Jalan Canang Emas 8, |
| City | Klang Selangor |
| Country | MY |
| Registration valid through | 2026 |
| Product codes listed | FRO, HDC, HIF, HRX, ITX, KGN, KXG, LGZ, MAX, NKB, PIF |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- None 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