FDA Device Establishments · JSON-LD · Markdown
FEI 3017252880 · Manufacture Medical Device · Status: Active
| FEI Number | 3017252880 |
|---|---|
| Owner / Operator | PMWCORPORATION (#10075535) |
| Address | Room A, 2F, 135, Cheoyongsaneop 3-gil, Cheongnyang-eup, Ulju-gun, Ulsan, 44988, KR |
| Mandatory US Agent | KMC USA, Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KXG |
| Regulation § (21 CFR) | 880.6025 |
| Proprietary names | SMART DIAGNOSTIC's FLOCKED SWAB SD304D; RADI Flocked Swab OD103NB; PARA FLOCKED SWAB GB946OP; PMW Flocked Swab PMW-SWAB NP1; PARA FLOCKED SWAB GB946DP; SMART DIAGNOSTIC's FLOCKED SWAB SD304O; PMW-SWAB PMW CONTROL SWAB; PMW Flocked Swab PMW-SWAB DUAL; RADI Flocked Swab OD103DB; RADI Flocked Swab OD103OB |
Source: openFDA. Public-domain (CC0).