Establishment registration
PLASTIFLEX HEALTHCARE DIVISION OF PLASTIFLEX GROUP NV
FDA establishment registration 3008331339 · Paal Beringen Limburg, BE
Key facts
| Registration number | 3008331339 |
|---|---|
| Establishment name | PLASTIFLEX HEALTHCARE DIVISION OF PLASTIFLEX GROUP NV |
| Owner/operator | Plastiflex Healthcare Division of Plastiflex Group NV |
| Owner/operator number | 10031967 |
| FEI number | 3008331339 |
| Address | Buntjesstraat 13 |
| City | Paal Beringen Limburg |
| Country | BE |
| Registration valid through | 2026 |
| Product codes listed | BZE, BZO |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 100–999 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