AccessGUDID - DEVICE: MARCH IFAK RESUPPLY (M6898130301110)

GUDID

Device Identifier (DI) Information

Brand Name: MARCH IFAK RESUPPLY
Version or Model: 11
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 81-303-01
Company Name: Safeguard US Operating, LLC

Primary DI Number: M6898130301110
Issuing Agency: HIBCC
Commercial Distribution End Date: December 31, 2028
Device Count: 1
Labeler D-U-N-S® Number*: 118492643 *Terms of Use

Device Description: The MARCH™ IFAK Resupply bundle is intended to be used as resupply for the US Army standard IFAK or similar commercial applications. Using the combat-proven practice of kit organization and standardization, the MARCH™ IFAK Resupply is designed to be used under the most adverse conditions. It uses MARCH™ medical gear in a color-coded trauma treatment system to treat the five leading causes of preventable death on the battlefield. It comes with quick reference cards to complete the system.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44047	First aid kit, non-medicated, single-use	A convenient collection of equipment and materials intended to be used in an emergency for the rapid, initial treatment of an injury. This device is typically used by emergency medical services (EMS), institutions, schools, the home, motor vehicles, and other public settings. This device does not contain medicinal substances/pharmaceuticals. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OHO	First Aid Kit Without Drug

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 33c75fd3-c99f-49db-a408-432abaee34c1
Public Version Date: August 19, 2025
Public Version Number: 2
DI Record Publish Date: February 19, 2025