FDA Device Establishments · JSON-LD · Markdown
FEI 3002646096 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device Repack or Relabel Medical Device · Status: Active
| FEI Number | 3002646096 |
|---|---|
| Owner / Operator | Oxford Gene Technology (IP) Limited (#9026291) |
| Address | Oxford Gene Technology, 418 Cambridge Science Park, Milton Road, CAMBRIDGE Cambridgeshire, CB4 0PZ, GB |
| Mandatory US Agent | OXFORD GENE TECHNOLOGY, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PPM |
| Regulation § (21 CFR) | 864.4010 |
| Proprietary names | CytoCell 8 Square Template Slides (PCN 008); CytoCell 24 Square Template Slides (PCN 007); CytoCell Porcelain Wash Jars (PCN 009); CytoCell DAPI Antifade Counterstain FS (DFS 500L, DFS 10ML); CytoCell DAPI Antifade Counterstain ES (DES 500L, DES 1000L, DES 10ML); CytoCell Hybridisation Chamber (PCN 004); CytoCell Rubber Solution Glue (PCA 005); CytoCell Mounting Medium (PCN 003); CytoCell Hybridisation Solution B (HB 500L, HB 1000L); CytoCell 20x SSC Buffer (PCA 003) |
Source: openFDA. Public-domain (CC0).