Establishment registration
GEBR. BRASSELER GMBH & CO. KG
FDA establishment registration 8010468 · LEMGO North Rhine-Westphalia, DE
Key facts
| Registration number | 8010468 |
|---|---|
| Establishment name | GEBR. BRASSELER GMBH & CO. KG |
| Owner/operator | GEBR. BRASSELER GMBH & CO. KG |
| Owner/operator number | 8010468 |
| FEI number | 3002806577 |
| Address | ATTN.: Petra Meier |
| City | LEMGO North Rhine-Westphalia |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DZA, DZE, DZI, DZP, EFB, EHJ, EHL, EHM, EIC, EIY, EJL, EKK, EKM, EKN, EKP, EKR, EKS, EKX, ELC, ELR, FSM, FZX, GFA, GFC, GFF, GWM, HBE, HRS, HTW, HTY and 20 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 1,000+ 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