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Mojo Combat Lifesaver Bag - Intermediate

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Mojo Combat Lifesaver Bag - Intermediate FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
The Mojo® Combat Lifesaver Bag uses MARCH™ medical gear in a user friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death on the battlefield. The Mojo® CLS bag is mission designed and highly versatile. It contains components for a warfighter with advanced individual or CLS training to treat multiple casualties at point of injury. FDA UDI
Model / Reference
09 FDA UDI
Description
The Mojo® Combat Lifesaver Bag uses MARCH™ medical gear in a user friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death on the battlefield. The Mojo® CLS bag is mission designed and highly versatile. It contains components for a warfighter with advanced individual or CLS training to treat multiple casualties at point of injury. FDA UDI

Identifiers

Catalog Number
83-323 FDA UDI
Primary DI / UDI-DI
M68983323090 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 Combat Lifesaver Bag - Intermediate 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48749dfc-b289-4d63-a7ba-8f1711800d9d 35 fields · synced May 30, 2026