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Mojo IFAK - Basic

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Mojo IFAK - Basic FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Mojo® IFAK uses a user-friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death in combat. The Mojo® IFAK is configurable and extremely versatile for every mission possibility. It can be worn in a drop leg configuration, and with the removable leg strap it can also attach directly to MOLLE vest/harness, or to a 2” duty/gun belt. FDA UDI
Model / Reference
08 FDA UDI
Description
Mojo® IFAK uses a user-friendly, color-coded trauma treatment system distinctly packaged with icon identifiers to treat the five preventable causes of death in combat. The Mojo® IFAK is configurable and extremely versatile for every mission possibility. It can be worn in a drop leg configuration, and with the removable leg strap it can also attach directly to MOLLE vest/harness, or to a 2” duty/gun belt. FDA UDI

Identifiers

Catalog Number
81-132-01 FDA UDI
Primary DI / UDI-DI
M6898113201080 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 IFAK - 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ded0035c-228d-4987-8aab-204352eb777e 35 fields · synced May 29, 2026