Duns Number:001180207
Device Description: 4 Shelf OSHA First Aid Station - Contains: Alcohol Pads, 100ct; Antacid Tablets, 50ct; An 4 Shelf OSHA First Aid Station - Contains: Alcohol Pads, 100ct; Antacid Tablets, 50ct; Antiseptic Spray, 4 oz; Antiseptic Wipes 25ct; Aspirin Tablets, 50ct; Burn Spray, 4 oz; Cotton Tipped Applicators, 100ct; Elastic Bandage Wrap, 4" x 5 yd; Extra-Strength Non-Aspirin Tablets, 50ct; Eyewash, 4oz, Sterile Eye Cup, 2 Eye Pads and Strips; First Aid Guide; First Aid/Burn Cream Packets, 25ct; Heavy Woven Fabric Bandages, 1" x 3", 50ct; Heavy Woven Fabric Bandages, 2" x 3", 25ct; Heavy Woven Fingertip Fabric Bandages, 25ct; Heavy Woven Knuckle Fabric Bandages, 25ct; Hema-Seal 8 x10 Trauma Pad in 4" x 4yd gauze, 2 Nitrile Exam Gloves; Ibuprofen Tablets, 50ct; Nitrile Exam Gloves, 10ct; Scissors; Sinus Tablets, 50ct; Sterile Gauze Bandage, 2" x 4 yd (2); Sterile Gauze Bandage, 4" x 4yd (2); 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.
Catalog Number
6175
Brand Name
First Aid Only
Version/Model Number
6175
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
LRR
Product Code Name
First Aid Kit With Drug
Public Device Record Key
4f01e3e9-ea17-460f-a387-d1588093c2ba
Public Version Date
April 15, 2021
Public Version Number
2
DI Record Publish Date
September 18, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 303 |