Establishment registration
A.HANDTE MEDIZINTECHNIK GMBH & CO. KG
FDA establishment registration 8010155 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010155 |
|---|---|
| Establishment name | A.HANDTE MEDIZINTECHNIK GMBH & CO. KG |
| Owner/operator | A.HANDTE MEDIZINTECHNIK GMBH & CO. KG |
| Owner/operator number | 8010155 |
| FEI number | 4476 |
| Address | EHRENBERGSTRASSE 39 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, ECR, EIG, EIL, EKB, EKE, EMI, EMJ, EMK, EML, EMM, ERL, FGN, FHL, FMA, FZO, FZS, FZY, GAC, GAD, GAI, GDG, GDI, GEG, GEJ, GFJ, GWY, HAO, HCY, HDL and 32 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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