Establishment registration
FCI FRANCE CHIRURGIE INSTRUMENTATION
FDA establishment registration 3002991496 · PARIS Ile-de-France, FR
Key facts
| Registration number | 3002991496 |
|---|---|
| Establishment name | FCI FRANCE CHIRURGIE INSTRUMENTATION |
| Owner/operator | Carl Zeiss Meditec AG (Jena) |
| Owner/operator number | 9053564 |
| FEI number | 3002991496 |
| Address | 20-22 RUE LOUIS ARMAND |
| City | PARIS Ile-de-France |
| Country | FR |
| Registration valid through | 2026 |
| Product codes listed | DQO, FFS, GEX, HJK, HJL, HJZ, HMX, HNC, HND, HNF, HNL, HNN, HNP, HNR, HNW, HOY, HPZ, HQB, HQF, HQN, HQX, JYJ, LZU, MML, MPA, MQU, MXY, NCB, NFM, NGY and 1 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 1,000+ 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