Identity
- Trade Name
- Mojo First Responder - Basic FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- The Mojo® First Responder Bag is a lightweight, highly capable kit that was developed to have the smallest possible cube while matching the capabilities of a standard Combat Lifesaver Bag. It is ideal for team, squad, and as a vehicle jump out bag. The Mojo® First Responder Bag is carried by an adjustable shoulder strap and attaches to MOLLE. It uses MARCH™ medical gear in a color-coded trauma treatment system to treat the five preventable causes of death on the battlefield. FDA UDI
- Model / Reference
- 07 FDA UDI
- Description
- The Mojo® First Responder Bag is a lightweight, highly capable kit that was developed to have the smallest possible cube while matching the capabilities of a standard Combat Lifesaver Bag. It is ideal for team, squad, and as a vehicle jump out bag. The Mojo® First Responder Bag is carried by an adjustable shoulder strap and attaches to MOLLE. It uses MARCH™ medical gear in a color-coded trauma treatment system to treat the five preventable causes of death on the battlefield. FDA UDI
Identifiers
- Catalog Number
- 83-301 FDA UDI
- Primary DI / UDI-DI
- M68983301070 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 First Responder - Basic by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as First aid kit, non-medicated, single-use.
- IFAK — FARETEC, INC. · Class I
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- Forward Tac-FAK Massive Hemorrhage (Tac-FAK M) — INTEGRATED MEDCRAFT LLC · Class I
- NAR — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI c9ae0d35-ef3e-46d9-8d78-c7783f190928 35 fields · synced Jun 8, 2026