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TOTAL RESOURCES INTERNATIONAL INC.

US

Last updated May 24, 2026

What TOTAL RESOURCES INTERNATIONAL INC. makes

The company produces medicated and non-medicated first aid kits designed for reusable applications, including trauma and emergency preparedness. Their portfolio also includes antimicrobial wound hydrogel dressings and irrigation solutions for wound care, as well as a non-bioabsorbable, non-antimicrobial haemostatic agent derived from plant polysaccharides.

These devices are classified under FDA’s Class I, N, and U categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Total Resources International Inc. manufacture?

Total Resources International Inc. specializes in first aid and wound care devices. Their portfolio includes medicated and non-medicated first aid kits, often designed for reusable use in trauma or emergency preparedness scenarios. They also produce antimicrobial wound hydrogel dressings and irrigation solutions for wound care, as well as a plant polysaccharide-based haemostatic agent that is non-bioabsorbable and non-antimicrobial.

Where is Total Resources International Inc. based?

The company is based in the United States. This location is relevant for regulatory compliance and distribution, as their devices are subject to FDA oversight.

Which regulatory registries list devices manufactured by Total Resources International Inc.?

Devices from Total Resources International Inc. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify device details.

How are the devices produced by Total Resources International Inc. classified under FDA regulations?

The company’s devices fall under FDA’s Class I, N (non-significant risk), and U (unclassified) categories. Class I devices are generally considered low-risk, often requiring only general controls for regulation, while N and U classifications may involve specific exemptions or additional oversight depending on the device’s intended use and risk profile.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
trikits.com
LinkedIn
—
Facebook
—
Phone
9095941220
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
790160535

Catalogue (71)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Be Smart Get Prepared 22EME06087REV1; 22EME06087REV2
FDA UDI
Class IActive
Be Smart Get Prepared 03HBC21073PK8
FDA UDI
Class IActive
Be Smart Get Prepared 10HBC01329GLRV1; 10HBC01329KROGER
FDA UDI
NActive
Be Smart Get Prepared 10OUT02086REV5
FDA UDI
NActive
Be Smart Get Prepared 10OUT02134REV1
FDA UDI
NActive
Be Smart Get Prepared 10HBC01172WM
FDA UDI
NActive
Be Smart Get Prepared 03HBC21174
FDA UDI
Class IActive
Be Smart Get Prepared 22EME06015
FDA UDI
Class IActive
Be Smart Get Prepared 22EME06081
FDA UDI
NActive
Be Smart Get Prepared 04HBC21061BOX
FDA UDI
UActive
Be Smart Get Prepared 10HDW05002; 10HDW05002HARBOR
FDA UDI
NActive
Be Smart Get Prepared 10OUT02099REV1
FDA UDI
NActive
Be Smart Get Prepared 10HBC01369
FDA UDI
NActive
Be Smart Get Prepared 10HBC01361REV1WAG
FDA UDI
NActive
Be Smart Get Prepared 22EME06099REV1
FDA UDI
NActive
Be Smart Get Prepared 10HDW05003
FDA UDI
NActive
Be Smart Get Prepared 10COM15008
FDA UDI
NActive
Be Smart Get Prepared 10AUT04055
FDA UDI
NActive
Be Smart Get Prepared 10OUT02141; 10OUT02141RECOM
FDA UDI
NActive
Be Smart Get Prepared 10OUT02029REV5
FDA UDI
NActive
Be Smart Get Prepared 10TRA451
FDA UDI
NActive

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