Establishment registration
VEHU MEDICAL INSTRUMENTE GMBH
FDA establishment registration 9616246 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9616246 |
|---|---|
| Establishment name | VEHU MEDICAL INSTRUMENTE GMBH |
| Owner/operator | VEHU MEDICAL INSTRUMENTE GMBH |
| Owner/operator number | 9040464 |
| FEI number | 3003052153 |
| Address | Dr. Karl-Storz-Strasse 25 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Manufacturer, Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | DWO, DWS, DZC, EAX, EBL, ECN, ECR, EFL, EIG, EIS, EJG, EKI, EME, EMF, EMG, EMH, EMI, EML, EMM, EMN, EPY, EZB, FAX, FBM, FFO, FFQ, FHA, FHQ, FNS, FNY and 79 more |
| Device classes | 1, 2 |
At a glance
- 100–999 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