IFAK RESUPPLY 81-304-01

GUDID M6898130401020

IFAK Resupply is designed to be used under the most adverse conditions. It uses medical gear in a color-coded trauma treatment system to treat the leading causes of preventable death in combat situations.

Safeguard US Operating, LLC

First aid kit, non-medicated, single-use

• Primary Device ID: M6898130401020
• NIH Device Record Key: 7d272d65-d273-4126-a363-50c24cf6d858
• Commercial Distribution Discontinuation: 2028-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IFAK RESUPPLY
• Version Model Number: 02
• Catalog Number: 81-304-01
• Company DUNS: 118492643
• Company Name: Safeguard US Operating, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M6898130401020 [Primary]

FDA Product Code

• OHO: First Aid Kit Without Drug

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-03-27
• Device Publish Date: 2025-02-19

On-Brand Devices [IFAK RESUPPLY]

• M6898130401020: IFAK Resupply is designed to be used under the most adverse conditions. It uses medical gear in
• M6898130401030: IFAK Resupply is designed to be used under the most adverse conditions. It uses medical gear in