FDA Device Establishments · JSON-LD · Markdown
FEI 3004404323 · Export Device to the United States But Perform No Other Operation on Device Foreign Private Label Distributor Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3004404323 |
|---|---|
| Owner / Operator | MACO PHARMA (#9067788) |
| Address | 233 RUE LORTHIOIS, --, MOUVAUX Hauts-de-France, 59420, FR |
| Mandatory US Agent | MACO PHARMA |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KSS |
| Regulation § (21 CFR) | 864.9050 |
| Proprietary names | 9MPSBI485: MacoPress Smart and DMS RS485 Module - with breaker for main press; 9MPSBR485: MacoPress Smart and DMS RS485 Module - no breaker; 9MPSBILAN: MacoPress Smart and DMS Ethernet Module - with breaker for main press; 9MPSBRLAN: MacoPress Smart and DMS Ethernet Module - no breaker; 9MPSBIWIFI: MacoPress Smart and DMS WiFi Module - with breaker for main press; 9MPSBRWIFI: MacoPress Smart and DMS WiFi Module - no breaker |
Source: openFDA. Public-domain (CC0).