FDA device listing
L-Type LDL-C Reagent
FDA device listing 1758184549 · FUJIFILM Wako Pure Chemical Corporation
Key facts
| Proprietary names | L-Type LDL-C Reagent |
|---|---|
| Owner/operator | FUJIFILM Wako Pure Chemical Corporation |
| Owner/operator number | 8030234 |
| Premarket submissions | K982271 |
| Product codes | MRR |
| Device names | MRR - System, Test, Low Density, Lipoprotein |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1475 |
| Review panels | Clinical Chemistry |
| Registered establishments | FUJIFILM Healthcare Manufacturing Corporation MIE Office, FUJIFILM Wako Pure Chemical Corporation Diagnostics Design Office (Amagasaki) |
| Establishment registrations | 3003419906, 3003522182 |
| FEI numbers | 3003419906, 3003522182 |
| Establishment operations | Manufacturer, Specification Developer |
| 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