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Uline 25 Person First Aid Kit - SUB

FDA UDI

Class N (US FDA UDI)

by Uline, Inc.

Identity

Trade Name
Uline 25 Person First Aid Kit - SUB FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
"(1) ABSORBENT COMPRESS (10) ANTIBIOTIC OINTMENT (10) ANTISEPTIC TOWELETTE (6) BURN CREAM (1) CPROTECTOR (1) EYE PAD (16) FABRIC BANDAGE (5) FABRIC FINGERTIP BANDAGE (4) FABRIC KNUCKLE BANDAGE (1) FIRST AID FACTS GUIDE (1) FIRST AID TAPE (1) PLASTIC TWEEZERS (4) GAUZE PAD (1) GAUZE ROLL (1) INSTANT ICE PACK (2) NITRILE GLOVE (16) PLASTIC BANDAGE (1) SCISSORS (1) SINGLE USE SALINE (1) TRIANGULAR BANDAGE" FDA UDI
Model / Reference
H-1293-S1 FDA UDI
Description
"(1) ABSORBENT COMPRESS (10) ANTIBIOTIC OINTMENT (10) ANTISEPTIC TOWELETTE (6) BURN CREAM (1) CPROTECTOR (1) EYE PAD (16) FABRIC BANDAGE (5) FABRIC FINGERTIP BANDAGE (4) FABRIC KNUCKLE BANDAGE (1) FIRST AID FACTS GUIDE (1) FIRST AID TAPE (1) PLASTIC TWEEZERS (4) GAUZE PAD (1) GAUZE ROLL (1) INSTANT ICE PACK (2) NITRILE GLOVE (16) PLASTIC BANDAGE (1) SCISSORS (1) SINGLE USE SALINE (1) TRIANGULAR BANDAGE" FDA UDI

Identifiers

Primary DI / UDI-DI
10850015055307 FDA UDI
FDA Product Code
LRR FDA UDI
KGX FDA UDI
EFQ FDA UDI
HMP FDA UDI
CBP FDA UDI
IMD FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
880.5240 FDA UDI
878.4440 FDA UDI
868.5870 FDA UDI
890.5710 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

No

FDA UDI

Category: First aid kit, medicatedAdhesive bandageNon-woven gauze padWound-nonadherent dressing, absorbent, non-antimicrobial

Uline 25 Person First Aid Kit - SUB by Uline, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endothermic cold therapy pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uline, Inc.

Sources (1)

  • FDA UDI 1f3ab78d-861a-4bd4-b6ed-073743cc7935 33 fields · synced Jun 8, 2026