FDA device listing
Basic First Aid Kit,Blood Borne Pathogen Kit,Burn Kit,Overdose Response Kit,Resuscitation Kit
FDA device listing 1042671836 · Redicare LLC
Key facts
| Proprietary names | Basic First Aid Kit,Blood Borne Pathogen Kit,Burn Kit,Overdose Response Kit,Resuscitation Kit |
|---|---|
| Owner/operator | Redicare LLC |
| Owner/operator number | 10053279 |
| 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 | REDICARE LLC |
| Establishment registrations | 3013034812 |
| FEI numbers | 3013034812 |
| Establishment operations | Specification Developer |
| 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