AccessGUDID - DEVICE: Medi-First 120 Piece Multi-Purpose Kit (00347682401207)

GUDID

Device Identifier (DI) Information

Brand Name: Medi-First 120 Piece Multi-Purpose Kit
Version or Model: 40120
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 40120
Company Name: Medique Products

Primary DI Number: 00347682401207
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 086911794 *Terms of Use

Device Description: 30 - Adhesive Bandages 1 in x 3 in 20 - Adhesive Bandages 3/8 in x 1-1/2 in 1 - Adhesive Tape Roll 1/2 in x 5 yd 1 - Triangular Bandage 40 in x 40 in x 56 in 10 - Cotton Tip Applicators 2 - Finger Splints 1 - First Aid Instruction Guide 4 - Sterile Gauze Dressing 2 in x 2 in 4 - Sterile Gauze Dressing 4 in x 4 in 1 - Sterile Trauma Pad 5 in x 9 in 1 - Gauze Roll 2 in x 4.1 yd 4 - Examination Gloves 1 - Instant Cold Compress 5 - Burn Cream Packets 6 - Antibiotic Ointment Packets 12 - Alcohol Prep Pads 3 - Sting Relief Pads 12 - Antiseptic Towelettes 1 - Metal Scissors 1 – 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: No 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
Special Storage Condition, Specify: Store at room temperature.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 41f134c0-d1d8-401b-b60f-7778fa8354a3
Public Version Date: August 01, 2019
Public Version Number: 1
DI Record Publish Date: July 24, 2019