First Aid Only - 100 Person 3 Shelf First Aid Kit with Steel - Acme United Corporation

Duns Number:001180207

Device Description: 100 Person 3 Shelf First Aid Kit with Steel Cabinet - Contains: Eyewash, 4oz, Sterile Eye 100 Person 3 Shelf First Aid Kit with Steel Cabinet - Contains: Eyewash, 4oz, Sterile Eye Cup, 2 Eye Pads and Strips; Alcohol Wipes, 100ct; Antiseptic Spray, 4 oz; Antiseptic Wipes, 25ct; Burn Spray, 4 oz; Cold Pack, 6" x 9"; Cotton Tipped Applicators, 100ct; Elastic Bandage Wrap, 4" x 5 yd; Extra-Strength Non-Aspirin Tablets, 50ct; First Aid Guide; First Aid/Burn Cream Packets, 25ct: Heavy Woven Fabric Bandages, 1" x 3", 50ct: Heavy Woven Fabric Bandages, 2" x 3", 10ct: Heavy Woven Fingertip Fabric Bandages, 25ct: Heavy Woven Knuckle Fabric Bandages, 25ct; Hema-Seal 8x10 Trauma Pad in 4" x 4 yd gauze, 2 Nitrile Exam Gloves; Nitrile Exam Gloves, 10ct; Scissors; Sterile Gauze Bandage, 2" x 4 yd; Sterile Gauze Bandage, 4" x 4 yd; Sterile Gauze Pads, 2" x 2", 10ct; Sterile Gauze Pads, 3" x 3", 10ct; Sterile Gauze Pads, 4" x 4", 10ct; Triangular Bandage, 40" x 40" x 56" (2); Triple Antibiotic Ointment Packets, 25ct; Triple Cut Adhesive Tape Roll, 2"; Tweezers.

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More Product Details

Catalog Number

6155

Brand Name

First Aid Only

Version/Model Number

6155

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

-

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

LRR

Product Code Name

First Aid Kit With Drug

Device Record Status

Public Device Record Key

b7844e02-1329-4bbc-b7cd-395ea8138755

Public Version Date

April 15, 2021

Public Version Number

2

DI Record Publish Date

September 17, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ACME UNITED CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 303