FDA Device Establishments · JSON-LD · Markdown
FEI 3010773581 · Manufacture Medical Device · Status: Active
| FEI Number | 3010773581 |
|---|---|
| Owner / Operator | Centron Corporation (#10045761) |
| Address | 44 Beolmal-ro, Dongan-gu, Anyang-si Gyeonggi, 14059, KR |
| Mandatory US Agent | CENTROVEST |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KSD |
| Regulation § (21 CFR) | 864.9750 |
| Proprietary names | TUBE SEALER SE640; TUBE SEALER SE340; TUBE SEALER SE540; TUBE SEALER SE470RS; TUBE SEALER SE530; TUBE SEALER SE330; TUBE SEALER SE170; TUBE SEALER SE160; TUBE SEALER SE7; TUBE SEALER SE9 |
Source: openFDA. Public-domain (CC0).