FDA device listing
FILTER SAMPLER Blood Serum Filter Standard Model,Fisherband Serum Filters Dispense+ Serum Filter,Fisherbrand Serum…
FDA device listing 2067863037 · Porex Corporation
Key facts
| Proprietary names | FILTER SAMPLER Blood Serum Filter Standard Model,Fisherband Serum Filters Dispense+ Serum Filter,Fisherbrand Serum Filters Dispense Filter System,Fisherbrand Serum Filters Instrument Specific Model,Fisherbrand Serum Filters Standard Model |
|---|---|
| Owner/operator | Porex Corporation |
| Owner/operator number | 1043678 |
| Product codes | GIM |
| Device names | GIM - Tubes, Vacuum Sample, With Anticoagulant |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1675 |
| Review panels | Clinical Chemistry |
| Registered establishments | POREX CORPORATION |
| Establishment registrations | 1043678 |
| FEI numbers | 1043678 |
| 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