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Mojo JFAK - Intermediate

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Mojo JFAK - Intermediate FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Mojo Medical Bags are equipped with MARCH Medical Gear in our simplified, color-coded treatment system linking icon identifiers to a treatment category within the MARCH protocol. MASSIVE HEMORRHAGE AIRWAY RESPIRATION CIRCULATION HEAD & HYPOTHERMIA FDA UDI
Model / Reference
02 FDA UDI
Description
Mojo Medical Bags are equipped with MARCH Medical Gear in our simplified, color-coded treatment system linking icon identifiers to a treatment category within the MARCH protocol. MASSIVE HEMORRHAGE AIRWAY RESPIRATION CIRCULATION HEAD & HYPOTHERMIA FDA UDI

Identifiers

Catalog Number
81-143 FDA UDI
Primary DI / UDI-DI
M68981143020 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
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 JFAK - Intermediate by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Safeguard Us Operating, Llc

Sources (1)

  • FDA UDI 777be36d-34ce-4570-8e78-7c0c5582c392 36 fields · synced May 30, 2026