FDA device listing
ACT Transfer Pipettes,AeroMed Transfer Pipettes,InfoLab Transfer Pipettes,Transfer Pipettes
FDA device listing 1083656969 · COPAN ITALIA Spa
Key facts
| Proprietary names | ACT Transfer Pipettes,AeroMed Transfer Pipettes,InfoLab Transfer Pipettes,Transfer Pipettes |
|---|---|
| Owner/operator | COPAN ITALIA Spa |
| Owner/operator number | 9016900 |
| Product codes | JRC |
| Device names | JRC - Micro Pipette |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | COPAN Diagnostics, Inc., COPAN DIAGNOSTICS, INC. |
| Establishment registrations | 2436875, 3017063217 |
| FEI numbers | 1000521444, 3017063217 |
| 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