Establishment registration
DRG INSTRUMENTS GMBH
FDA establishment registration 3002800697 · MARBURG Hesse, DE
Key facts
| Registration number | 3002800697 |
|---|---|
| Establishment name | DRG INSTRUMENTS GMBH |
| Owner/operator | BIOCHECK, INC. |
| Owner/operator number | 9033543 |
| FEI number | 3002800697 |
| Address | FRAUENBERGSTRASSE 18 |
| City | MARBURG Hesse |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | CDA, CDP, CDX, CDZ, CEC, CEP, CEW, CFL, CFP, CFT, CGF, CGI, CGJ, CGR, CHA, CHP, CIZ, CKG, CZS, DBM, DCK, DDC, DEG, DFQ, DGC, DHR, DPA, GGT, GMO, GNH and 69 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 100–999 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