Establishment registration
Fabryka Narzedzi Medycznych CHIRMED Marcin Dyner Spolka Komandytowa
FDA establishment registration 3005587147 · RUDNIKI K/CZESTOCHOWY Slaskie, PL
Key facts
| Registration number | 3005587147 |
|---|---|
| Establishment name | Fabryka Narzedzi Medycznych CHIRMED Marcin Dyner Spolka Komandytowa |
| Owner/operator | Fabryka Narzedzi Medycznych CHIRMED Marcin Dyner Spolka Koma |
| Owner/operator number | 9023253 |
| FEI number | 3005587147 |
| Address | UL. MSTOWSKA 8 A |
| City | RUDNIKI K/CZESTOCHOWY Slaskie |
| Country | PL |
| Registration valid through | 2026 |
| Product codes listed | DZC, DZM, EAX, ECP, EFL, EIB, EIX, EJI, EKC, EMH, EMJ, EMN, EMO, EMQ, FHQ, FMA, FXR, FYI, FZS, GAD, GAF, GCC, GDX, GDZ, HDF, HTC, HTD, HTE, HTF, HTR and 14 more |
| Device classes | 1, 2 |
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