FDA device listing
MiniCollect Complete K2E EDTA K2,MiniCollect Tube K2E EDTA K2
FDA device listing 1872818343 · GREINER BIO-ONE NA
Key facts
| Proprietary names | MiniCollect Complete K2E EDTA K2,MiniCollect Tube K2E EDTA K2 |
|---|---|
| Owner/operator | GREINER BIO-ONE NA |
| Owner/operator number | 8020040 |
| Premarket submissions | K182078 |
| Product codes | JKA |
| Device names | JKA - Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1675 |
| Review panels | Clinical Chemistry |
| Registered establishments | GREINER BIO-ONE GMBH |
| Establishment registrations | 8020040 |
| FEI numbers | 3000974732 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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