FDA device listing
Sedimentation Rate Tube
FDA device listing 1349190265 · CITOTEST LABWARE MANUFACTURING CO., LTD.
Key facts
| Proprietary names | Sedimentation Rate Tube |
|---|---|
| Owner/operator | CITOTEST LABWARE MANUFACTURING CO., LTD. |
| Owner/operator number | 9077486 |
| Product codes | GHC |
| Device names | GHC - Tube, Sedimentation Rate |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.6700 |
| Review panels | Hematology |
| Registered establishments | CITOTEST Labware Manufacturing CO., LTD. |
| Establishment registrations | 3010420046 |
| FEI numbers | 3010420046 |
| Establishment operations | Manufacturer |
| 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