AccessGUDID - DEVICE: First Aid Only (00092265249973)

GUDID

Device Identifier (DI) Information

Brand Name: First Aid Only
Version or Model: 249-O/P
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 249-O/P
Company Name: Acme United Corporation

Primary DI Number: 00092265249973
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001180207 *Terms of Use

Device Description: 200 Person 5 Shelf First Aid Industrial Metal Cabinet With Pocket Liner - Contains: Aspirin Tablets, 100 ct; Burn Gel Packets, 25 ct; Burn Spray, 4 oz; Butterfly Closures, 16 ct; Cold Pack, 4" x 5"; Cold Pack, 6" x 9"; Conforming Gauze Rolls, 2", 4 ct; Cotton Tipped Applicators, 100 ct (vial); CPR Face Shield, 2 Nitrile Exam Gloves and 2 BZK Towelettes; Extra-Strength Non-Aspirin Tablets, 250 ct; Eyewash, 0.5 oz; Eyewash, 4 oz; Eyewash, 8 oz ; Fingertip Fabric Bandages, 40 ct; First Aid Guide; Heavy Woven Fingertip Fabric Bandages, 25 ct; Hema-Seal 8 x10 Trauma Pad in 4" x 4 yd gauze, 2 Nitrile Exam Gloves; Hydrocortisone Cream Packets, 2 ct; Ibuprofen Tablets, 250 ct; Knuckle Fabric Bandages, 40 ct; Lister Bandage Shears, 5.5"; Nitrile Exam Gloves, 10 ct; Non Stick Pads, 3" x 4", 50 ct; Povidone-Iodine Infection Control Wipes, 50 ct; Spray-on Bandage, 3 oz; Sterile Eye Pads and Strips, 4 ct; Sterile Gauze Pads, 2" x 2" and 3" x 3", 48 ct; Sterile Gauze Pads, 4" x 4", 4 ct;Trauma Pad, 5" x 9", 2 ct; Triangular Bandage, 40" x 40" x 56", 2 ct; Triple Antibiotic Ointment Packets, 25 ct; Triple Cut Adhesive Tape Roll, 2"; Tweezers.

Device Characteristics

What MRI safety information does the labeling contain?	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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	Yes
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44039	First aid kit, medicated	A convenient collection of equipment, materials and pharmaceuticals intended to be used in an emergency for the rapid, initial treatment of an injury. It is typically used by emergency medical services (EMS), hospitals, institutions, schools, and other public settings. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LRR	First Aid Kit With Drug

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 589614e1-1836-4cc5-84df-c540076b7aad
Public Version Date: April 15, 2021
Public Version Number: 2
DI Record Publish Date: September 16, 2020