FDA Device Establishments · JSON-LD · Markdown
FEI 1317268 · Repack or Relabel Medical Device Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 1317268 |
|---|---|
| Owner / Operator | Life Technologies Corporation (#9915045) |
| Address | 3175 STALEY ROAD, GRAND ISLAND, NY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KIQ |
| Regulation § (21 CFR) | 864.2260 |
| Proprietary names | MarrowMAX Bone Marrow Medium(12260001); AmnioMAX C-100 Supplement(12556023); AmnioMAX C-100 Basal Medium(17001082); KaryoMAX Colcemid Solution in HBSS(15210040); KaryoMAX Colcemid Solution in PBS(15212012); PB-MAX Karyotyping Medium(12557021); PB-MAX Karyotyping Medium(12557013); AmnioMAX C-100 Supplement(12556015); AmnioMAX C-100 Basal Medium(17001074); MarrowMAX Bone Marrow Medium(12260014) |
Source: openFDA. Public-domain (CC0).