FDA device listing
Cederroth First Aid Cabinet,Cederroth First Aid Station,Green Guard Deluxe Trauma Kit,Green Guard Deluxe Vehicle…
FDA device listing 1997571428 · UniFirst First Aid Corporation
Key facts
| Proprietary names | Cederroth First Aid Cabinet,Cederroth First Aid Station,Green Guard Deluxe Trauma Kit,Green Guard Deluxe Vehicle Kit,Green Guard Fanny Pack,Green Guard First Responder Kit,Green Guard Five- Shelf Cabinet,Green Guard Four- Shelf Cabinet,Green Guard Four- Shelf Wide Cabinet,Green Guard Medium Vehicle Kit,Green Guard Small Vehicle Kit,Green Guard Super Utility Kit,Green Guard Three- Shelf… |
|---|---|
| Owner/operator | UniFirst First Aid Corporation |
| Owner/operator number | 9005674 |
| 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 | Medique Products |
| Establishment registrations | 1420763 |
| FEI numbers | 1833338 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| 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