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Micro Trauma Kit - Basic

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Micro Trauma Kit - Basic FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Your Mojo Medical Bag is equipped with MARCH Medical Gear featuring simple treatment icons and color-coding below: MASSIVE HEMORRAHAGE AIRWAY RESPIRATION CIRCULATION HEAD & HYPOTHERMIA FDA UDI
Model / Reference
01 FDA UDI
Description
Your Mojo Medical Bag is equipped with MARCH Medical Gear featuring simple treatment icons and color-coding below: MASSIVE HEMORRAHAGE AIRWAY RESPIRATION CIRCULATION HEAD & HYPOTHERMIA FDA UDI

Identifiers

Catalog Number
88-140 FDA UDI
Primary DI / UDI-DI
M68988140010 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

No

FDA UDI

Over-the-Counter

Yes

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

Micro Trauma Kit - 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 49dd1b17-4d8d-4887-8f7f-4a6b1db64213 35 fields · synced Jun 1, 2026