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Public Access Kit Individual

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Public Access Kit Individual FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
1 - SWAT-T Tourniquet 1 - Emergency Blanket 1 - Positional Airway Instruction Card 1 - Exam Gloves 1 - Sterile Abdominal Pad 8" x 10" 1 - Quick Reference Guide 2 - Rolled Gauze FDA UDI
Model / Reference
01 FDA UDI
Description
1 - SWAT-T Tourniquet 1 - Emergency Blanket 1 - Positional Airway Instruction Card 1 - Exam Gloves 1 - Sterile Abdominal Pad 8" x 10" 1 - Quick Reference Guide 2 - Rolled Gauze FDA UDI

Identifiers

Primary DI / UDI-DI
M68987220010 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
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Public Access Kit Individual by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 431bd9a6-53be-4bee-a144-690d59e6988f 35 fields · synced May 30, 2026