FDA Device Establishments · JSON-LD · Markdown
FEI 3002622561 · Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3002622561 |
|---|---|
| Owner / Operator | Promega Corporation (#9036108) |
| Address | 2800 Woods Hollow Road, Madison, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PPM |
| Regulation § (21 CFR) | 864.4010 |
| Proprietary names | 5X PCR Buffer C; Internal Lane Standard 600; DNA Polymerase I Klenow Fragment; GoTaq Green Master Mix; T4 DNA Ligase; BenchTop PhiX174 DNA/Hae III Markers; dUTP, 100mM; RNase ONE Ribonuclease; 25bp DNA Step Ladder; Abbott mSample Preparation System Bulk mLysisDNA Buffer Kit |
Source: openFDA. Public-domain (CC0).