FDA device listing
MPM-Bleed-Advanced,MPM-BOO-BOO Kit,MPM-DR Duece Med Kit,MPM-EMSISD-Rapid Response…
FDA device listing 1320553372 · M-Pak, Inc.
Key facts
| Proprietary names | MPM-Bleed-Advanced,MPM-BOO-BOO Kit,MPM-DR Duece Med Kit,MPM-EMSISD-Rapid Response Kit,MPM-EMSISD-TAC-MED-KIT,MPM-FWPD-Tac Med Kit-V1,MPM-HSG Reflex IFAK-Black,MPM-JPS-IFAK,MPM-R40-Med Kit,MPM-R60-Med Kit,MPM-Squad Medical Kit,MPM-TDA-Bandage Kit |
|---|---|
| Owner/operator | M-Pak, Inc. |
| Owner/operator number | 10089224 |
| Product codes | OHO |
| Device names | OHO - First Aid Kit Without Drug |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4014 |
| Review panels | General & Plastic Surgery |
| Registered establishments | M-PAK, INC. |
| Establishment registrations | 3017382111 |
| FEI numbers | 3017382111 |
| Establishment operations | 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