Establishment registration
MedDev Manufacturing Sdn Bhd
FDA establishment registration 3006307105 · Klang Selangor, MY
Key facts
| Registration number | 3006307105 |
|---|---|
| Establishment name | MedDev Manufacturing Sdn Bhd |
| Owner/operator | SeeBreath AB |
| Owner/operator number | 10041602 |
| FEI number | 3006307105 |
| Address | 2nd Floor, Lot 2552, Wisma Kierie, Jalan Seruling 59, |
| City | Klang Selangor |
| Country | MY |
| Registration valid through | 2026 |
| Product codes listed | CCK |
| 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