Establishment registration
EFINGER INSTRUMENTS GmbH & Co. KG
FDA establishment registration 9615004 · SPAICHINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9615004 |
|---|---|
| Establishment name | EFINGER INSTRUMENTS GmbH & Co. KG |
| Owner/operator | EFINGER INSTRUMENTS GMBH & Co. KG |
| Owner/operator number | 9033589 |
| FEI number | 3001130644 |
| Address | MAX-PLANCK-STRASSE 36 |
| City | SPAICHINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | FCL, GAB, GDM, GZX, HAE, HAO, HNL, HNW, HTD, HTX, HWQ, JOL, JYR, JYW, JZB, KAD, KAE, KAK, KAO, KAS, KAW, KAX, KAY, KBB, KBD, KBS, KBT, KTF, LRC, LRW and 6 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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