FDA device listing
Trauma Kits
FDA device listing 1754070115 · CERTIFIED SAFETY MFG., INC.
Key facts
| Proprietary names | Trauma Kits |
|---|---|
| Owner/operator | CERTIFIED SAFETY MFG., INC. |
| Owner/operator number | 9010174 |
| Premarket submissions | K940249 |
| Product codes | LRR |
| Device names | LRR - First Aid Kit With Drug |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.LRR |
| Review panels | General & Plastic Surgery |
| Registered establishments | CERTIFIED SAFETY MFG., INC. |
| Establishment registrations | 1932902 |
| FEI numbers | 1000158435 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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