Pocket Trauma Kit Basic 88-103-01

GUDID M6898810301020

First Responder kits are intended to be carried and used by dedicated non-medical First Responders. Vacuum-seal trauma treatment kit, designed for complete trauma treatment. This kit includes instructions and interventions to address immediate threats to life from massive hemorrhage, airway compromise, and respiratory effect from chest trauma, lacerations, and hypothermia. It slips easily into your cargo pocket and ensuring you have trauma management directly at the point of injury.

Safeguard US Operating, LLC

First aid kit, non-medicated, single-use

• Primary Device ID: M6898810301020
• NIH Device Record Key: c5c1ecca-f189-467f-99f9-334c47bd985d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pocket Trauma Kit Basic
• Version Model Number: 02
• Catalog Number: 88-103-01
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 855-428-6074
• Email: sales@safeguardmedical.com
• Phone: 855-428-6074
• Email: sales@safeguardmedical.com
• Phone: 855-428-6074
• Email: sales@safeguardmedical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M6898810301020 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-09
• Device Publish Date: 2026-01-30

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