Establishment registration
CM INSTRUMENTE GMBH
FDA establishment registration 9680518 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9680518 |
|---|---|
| Establishment name | CM INSTRUMENTE GMBH |
| Owner/operator | CM INSTRUMENTE GMBH |
| Owner/operator number | 9009573 |
| FEI number | 3005304066 |
| Address | GANSACKER 56 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BSY, CBH, CCW, DWS, DZC, EAX, EBL, EFL, EGN, EIG, EJG, EMF, EMG, EMI, EMJ, EPE, EPY, EXX, FAX, FFN, FFO, FFQ, FGM, FHA, FHQ, FMA, FMP, FNS, FNY, FSM and 129 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- None 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