Establishment registration
PAJUNK GMBH MEDIZINTECHNOLOGIE
FDA establishment registration 9611612 · GEISINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9611612 |
|---|---|
| Establishment name | PAJUNK GMBH MEDIZINTECHNOLOGIE |
| Owner/operator | PAJUNK GmbH Medizintechnologie |
| Owner/operator number | 8010639 |
| FEI number | 3002807847 |
| Address | KARL-HALL-STRASSE 01 |
| City | GEISINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BSN, BSO, BSP, BXN, CAZ, DYB, EIC, FCG, FGB, FMJ, GCJ, GDF, GDZ, GEI, GXD, GXI, GZI, GZJ, HAW, HCC, HET, HIH, HMX, IPF, IWJ, KDC, KGX, KNW, MDM, MJG and 4 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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