Establishment registration
ROSE GMBH FUER MEDIZINTECHNIK
FDA establishment registration 3002808022 · Trier Rhineland-Palatinate, DE
Key facts
| Registration number | 3002808022 |
|---|---|
| Establishment name | ROSE GMBH FUER MEDIZINTECHNIK |
| Owner/operator | Rose GmbH fuer Medizintechnik |
| Owner/operator number | 10042910 |
| FEI number | 3002808022 |
| Address | Gottbillstrasse 25 |
| City | Trier Rhineland-Palatinate |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BTO, DZI, ERL, FDF, FEQ, FQH, FRN, FTL, GAA, GAD, GAZ, GBX, GEH, GEI, GFD, GWM, HAW, HBC, HBE, HGP, HMX, HND, HNF, HNR, HQB, HQF, HRX, HRY, HSD, HSX and 38 more |
| Device classes | 1, 2, 3 |
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