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Public Access Advanced Kit

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
PUBLIC ACCESS ADVANCED KIT FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
(1) TMT (Tactical Mechanical Tourniquet) (1) Celox B-Con (1) Dual Seal Occlusive Dressing (1) Mini Compression Dressing (2) TACGAUZE (1) Emergency Blanket (2) Pair Vinyl Gloves (1) Klever Kutter (1) Permanent Marker (1) Emergency Instructions FDA UDI
Model / Reference
01 FDA UDI
Description
(1) TMT (Tactical Mechanical Tourniquet) (1) Celox B-Con (1) Dual Seal Occlusive Dressing (1) Mini Compression Dressing (2) TACGAUZE (1) Emergency Blanket (2) Pair Vinyl Gloves (1) Klever Kutter (1) Permanent Marker (1) Emergency Instructions FDA UDI

Identifiers

Catalog Number
SH-PSS-TMT-SM FDA UDI
Primary DI / UDI-DI
M689SHPAATMTSM010 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

No

FDA UDI

Over-the-Counter

Yes

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

Public Access Advanced Kit 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 28158dd4-64a9-4cae-af9f-809eaaf29f8b 35 fields · synced May 30, 2026