AccessGUDID - DEVICE: First Aid Only (00092265324625)

GUDID

Device Identifier (DI) Information

Brand Name: First Aid Only
Version or Model: FA-462
Commercial Distribution Status: In Commercial Distribution
Catalog Number: FA-462
Company Name: Acme United Corporation

Primary DI Number: 00092265324625
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001180207 *Terms of Use

Device Description: Consumer First Aid Kit, Soft pack Emergency Survival - with 223 pieces including: Adhesive Plastic Bandages, 1" x 3" (8), Adhesive Plastic Bandages, 2" x 4" (6), Adhesive Plastic Bandages, 3/4" x 3" (25), Adhesive Plastic Bandages, 3/8" x 1.5" (10), Alcohol Pads (10), Allergy Tablets (2), Antacid Tablets (4), Aspirin Tablets (4), Burn Gel Packets (2), Butterfly Wound Closures (8), BZK Antiseptic wipes (9); Castile Soap Towelettes (6), Cold Pack, 4" x 5", Conforming Gauze Roll, 2" (2), Cotton Tipped Applicators (2), Digital Thermometer, Elastic Bandage Wrap, 3" x 5 yd, Emergency Food Bars (6), Emergency Sleeping Bag, 36" x 84"; Emergency Water Packets, 4oz (2), Extra-Strength Non-Aspirin Tablets (4), Eyewash, 2 x 1oz, Finger Splint/Tongue Depressors (2), Fingertip Fabric Bandages (2), First Aid Guide, First Aid Tape, 1" x 10 yds, Tweezers, Ibuprofen Tablets (4), Knuckle Fabric Bandages (2), Lip Balm Packets (2), Lister Bandage Shears, 5.5", Moleskin (Blister Prevention), 2" x 2" (3), Motion Sickness Tablets (4), Nitrile Exam Gloves (2); Non-Stick Pad with Adhesive Tabs, 3" x 4" (2); Non-Stick Pads, 2" x 3" (2); Povidone-Iodine Infection Control Wipes (3); Safety Pins (2); Sterile Eye Pad; Sterile Gauze Pads, 2" x 2" (6), Sterile Gauze Pads, 3" x 3" (4), Sting Relief Wipes (3), Sunscreen Lotion Packet, Transparent Dressing, 2.375" x 2.75" (4), Trauma Pads, 5" x 9" (2), Triangular Bandage, 40" x 40" x 56", Triple Antibiotic Ointment Packet, Waterproof Matches (50)

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: 8a6fc7dd-85f6-47a4-b162-c09729db4ab8
Public Version Date: April 15, 2021
Public Version Number: 2
DI Record Publish Date: December 30, 2020