Establishment registration
RICHARD WOLF GMBH
FDA establishment registration 9611102 · KNITTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9611102 |
|---|---|
| Establishment name | RICHARD WOLF GMBH |
| Owner/operator | RICHARD WOLF GMBH |
| Owner/operator number | 8010049 |
| FEI number | 3002808001 |
| Address | PFORZHEIMER STR. 32 |
| City | KNITTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | BWB, BWN, CAM, CCQ, CCW, DRI, EIG, EOB, EOQ, EPT, EPY, EQH, EQL, ERL, EWY, EXQ, EXY, EZO, FAJ, FAS, FAX, FBM, FBN, FBO, FBP, FBQ, FCL, FCT, FCW, FCX and 137 more |
| Device classes | 1, 2 |
At a glance
- 100–999 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