Establishment registration
BENTEC Endoscopy GmbH
FDA establishment registration 1000343527 · Rietheim-Weilheim Baden-Wurttemberg, DE
Key facts
| Registration number | 1000343527 |
|---|---|
| Establishment name | BENTEC Endoscopy GmbH |
| Owner/operator | BENTEC Endoscopy GmbH |
| Owner/operator number | 10053828 |
| FEI number | 1000343527 |
| Address | Hinteres Oeschle 6 |
| City | Rietheim-Weilheim Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | FGA, GCP, GWG, OCZ |
| 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