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Uline Burn Kit - Single Use

FDA UDI

Class N (US FDA UDI)

by Uline, Inc.

Identity

Trade Name
Uline Burn Kit - Single Use FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
BURN GEL, FIRST AID FACTS GUIDE, FIRST AID TAPE, GAUZE BANDAGE COMPRESS, INSTANT ICE PACK, NITRILE GLOVES, NON-STICK PADS, 1 X 3" PLASTIC BANDAGES, 2 X 3" PLASTIC BANDAGES, RESCUE BLANKET, BURN DRESSING - 4 X 4", BURN DRESSING - 4 X 16" FDA UDI
Model / Reference
H-4172 FDA UDI
Description
BURN GEL, FIRST AID FACTS GUIDE, FIRST AID TAPE, GAUZE BANDAGE COMPRESS, INSTANT ICE PACK, NITRILE GLOVES, NON-STICK PADS, 1 X 3" PLASTIC BANDAGES, 2 X 3" PLASTIC BANDAGES, RESCUE BLANKET, BURN DRESSING - 4 X 4", BURN DRESSING - 4 X 16" FDA UDI

Identifiers

Catalog Number
H-4172 FDA UDI
Primary DI / UDI-DI
10851253007691 FDA UDI
FDA Product Code
LRR FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid kit, medicated

Uline Burn Kit - Single Use by Uline, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uline, Inc.

Sources (1)

  • FDA UDI d66d3f75-d700-45d5-8e10-b2819a7c7ecc 34 fields · synced May 30, 2026