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Individual Trauma Kit - Basic

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Individual Trauma Kit - Basic FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
1 - Celox Rapid 3"x 5' 1 - Swat-Tourniquet 1 - FoxSeal 1 - Positional Airway Instruction Card 1 - Rolled Gauze 1 - Compression Dressing 1 - Emergency Blanket 2 - Exam Gloves 1 - Quick Reference Guide FDA UDI
Model / Reference
05 FDA UDI
Description
1 - Celox Rapid 3"x 5' 1 - Swat-Tourniquet 1 - FoxSeal 1 - Positional Airway Instruction Card 1 - Rolled Gauze 1 - Compression Dressing 1 - Emergency Blanket 2 - Exam Gloves 1 - Quick Reference Guide FDA UDI

Identifiers

Catalog Number
87-100-01 FDA UDI
Primary DI / UDI-DI
M6898710001050 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

Yes

FDA UDI

Over-the-Counter

No

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

Individual 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 35f05473-9546-4412-94bf-1d90cf56d9ab 35 fields · synced Jun 1, 2026