FDA device listing
DAKO EOSIN,Dako Eosin Y Phloxine B,Dako Modified Eosin Y
FDA device listing 2031618655 · Agilent Technologies, Inc
Key facts
| Proprietary names | DAKO EOSIN,Dako Eosin Y Phloxine B,Dako Modified Eosin Y |
|---|---|
| Owner/operator | Agilent Technologies, Inc |
| Owner/operator number | 10038794 |
| Product codes | HYB |
| Device names | HYB - Eosin Y |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.1850 |
| Review panels | Hematology |
| Registered establishments | Agilent Technologies Denmark ApS, Agilent Technologies Inc., ATSI Logistics Center ApS |
| Establishment registrations | 9610099, 3009189893, 3013059683 |
| FEI numbers | 3002806778, 3009189893, 3013059683 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Repackager/Relabeler, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database