Uline ANSI Approved First Aid Kit - Class A, 25 Person - "(2) ABSORBENT COMPRESS(10) ANTIBIOTIC - ULINE, INC.

Duns Number:039612668

Device Description: "(2) ABSORBENT COMPRESS(10) ANTIBIOTIC OINTMENT(10) ANTISEPTIC TOWELETTES(10) BURN CREAM(1 "(2) ABSORBENT COMPRESS(10) ANTIBIOTIC OINTMENT(10) ANTISEPTIC TOWELETTES(10) BURN CREAM(1) BURN DRESSING(1) CPROTECTOR(8) EYE PAD WITH TAPE(1) FIRST AID FACTS GUIDE(1) FIRST AID TAPE(4) GAUZE PADS(1) GAUZE ROLL(10) HAND SANITIZER(1) INSTANT ICE PACK(2) NITRILE GLOVES(16) PLASTIC BANDAGES (1) SCISSORS(1) SINGLE USE SALINE(1) TRIANGULAR BANDAGE"

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More Product Details

Catalog Number

H-6469

Brand Name

Uline ANSI Approved First Aid Kit - Class A, 25 Person

Version/Model Number

H-6469

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

CBP

Product Code Name

Valve, Non-Rebreathing

Device Record Status

Public Device Record Key

431dd271-f1af-4955-a2b9-75d825538173

Public Version Date

March 23, 2022

Public Version Number

6

DI Record Publish Date

January 18, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ULINE, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 8
2 A medical device with a moderate to high risk that requires special controls. 1
U Unclassified 2