Establishment registration
BIS MASTERMED
FDA establishment registration 3030451558 · Kosice Kosicky, SK
Key facts
| Registration number | 3030451558 |
|---|---|
| Establishment name | BIS MASTERMED |
| Owner/operator | BIS MASTERMED s.r.o. |
| Owner/operator number | 10089528 |
| FEI number | 3030451558 |
| Address | Juzna trieda 119 |
| City | Kosice Kosicky |
| Country | SK |
| Registration valid through | 2026 |
| Product codes listed | GEN, HLF, HLN, HMQ, HMR, HMX, HMZ, HNA, HNB, HNC, HND, HNF, HNG, HNH, HNI, HNJ, HNK, HNL, HNM, HNN, HNP, HNQ, HNR, HNW, HNX, HNY, HNZ, HOB, HOC, HOD and 3 more |
| Device classes | 1 |
At a glance
- 10–99 Device listings
- None 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