Identity
- Trade Name
- Mojo Direct Action - Basic FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- The Mojo® Direct Action Aid Bag strikes the balance between smaller Combat Lifesaver bags and bulkier advanced care bags. This ultra low profile, multi-mission medical bag is designed for use in close quarters and vehicle environments. The pockets, flaps, pouches and multi-loop retention system allow for maximum configuration options for a variety of patrol, assault, rescue and vehicle-based missions. Inside the Direct Action Aid Bag are clear, removable pockets that allow for quick, organized treatments using medical gear in a user-friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death in combat FDA UDI
- Model / Reference
- 11 FDA UDI
- Description
- The Mojo® Direct Action Aid Bag strikes the balance between smaller Combat Lifesaver bags and bulkier advanced care bags. This ultra low profile, multi-mission medical bag is designed for use in close quarters and vehicle environments. The pockets, flaps, pouches and multi-loop retention system allow for maximum configuration options for a variety of patrol, assault, rescue and vehicle-based missions. Inside the Direct Action Aid Bag are clear, removable pockets that allow for quick, organized treatments using medical gear in a user-friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death in combat FDA UDI
Identifiers
- Catalog Number
- 84-495-01 FDA UDI
- Primary DI / UDI-DI
- M68984495010110 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- First aid kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, non-medicated, single-use
Mojo Direct Action - Basic by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 25dd17a3-1b4f-41fd-8004-7d55d485649f 35 fields · synced May 30, 2026