Establishment registration
GUENTER BISSINGER MEDIZINTECHNIK GMBH
FDA establishment registration 8010456 · TENINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010456 |
|---|---|
| Establishment name | GUENTER BISSINGER MEDIZINTECHNIK GMBH |
| Owner/operator | GUENTER BISSINGER MEDIZINTECHNIK GMBH |
| Owner/operator number | 8010456 |
| FEI number | 3002477156 |
| Address | Hans-Theisen-Str. 1 |
| City | TENINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | FHQ, GCJ, GDZ, GEI, GEN, GZX, HET, HNF, HNR, HWA, JOL, KNF, KNS, NAY, NNI |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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