Identity
- Trade Name
- Mojo Direct Action Bag - Intermediate FDA UDI
- Generic Name
- First aid kit, medicated FDA UDI
- Device Name
- Equips trained medical first responders with a higher density of the core components identified by the CoTCCC as required to provide lifesaving interventions through buddy-aid and medical aid tasks during the Tactical Field Care phase of care. • The system is color coded and sequentially organized for rapid visual and muscle • memory identification of the appropriate tool required under the MARCH protocol. • The system has an “open architecture” which allows the introduction of emerging technologies that improve the lifesaving capabilities of the individual. FDA UDI
- Model / Reference
- 01 FDA UDI
- Description
- Equips trained medical first responders with a higher density of the core components identified by the CoTCCC as required to provide lifesaving interventions through buddy-aid and medical aid tasks during the Tactical Field Care phase of care. • The system is color coded and sequentially organized for rapid visual and muscle • memory identification of the appropriate tool required under the MARCH protocol. • The system has an “open architecture” which allows the introduction of emerging technologies that improve the lifesaving capabilities of the individual. FDA UDI
Identifiers
- Catalog Number
- 84-493 FDA UDI
- Primary DI / UDI-DI
- M68984493010 FDA UDI
- FDA Product Code
- LRR FDA UDI
- GMDN Term
- First aid kit, medicated FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- Not 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
Mojo Direct Action Bag - Intermediate by Safeguard Us Operating, Llc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 N | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 12a04920-f198-44d2-a04c-0f7443e7b029 36 fields · synced May 30, 2026