AccessGUDID - DEVICE: Medi-First Plus Large Vehicle Metal First Aid Kit (00347682929015)

GUDID

Device Identifier (DI) Information

Brand Name: Medi-First Plus Large Vehicle Metal First Aid Kit
Version or Model: 929M1
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 929M1
Company Name: Medique Products

Primary DI Number: 00347682929015
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 086911794 *Terms of Use

Device Description: 19818 - STD 1 EACH Mediwash eyewash 4oz 24402 – 1 EACH MF Antiseptic Spray 2oz Pump 22502 – 1 EACH MF Burn Spray Pump 2oz 221B - 0.002 M ALCOHOL PREP PADS-BULK 223B - 0.003 M MF TRIPLE ANTIBIOTIC .5gr BULK 60501 – 1 EACH 2" StrleConformGauze1s 60612 - STD 1 EACH 2"x2" Sterile Gauze Pad10s 60701 – 1 EACH Adhesive Tape 1/2 x5 yd 61450 – 1 EACH HW 7/8"X3" Woven Strip 50s 64101 - 1 EACH Bloodstopper Compress 9X5 (1s) 643B - 0.005 M HW Latex Free Woven Fingertip BULK 645B - 0.005 M HW Latex Free Woven Knuckle BULK 65001 - 1 EACH Tri cut Bandage non-sterile 1s + pins 75599 - 2 EACH Disposable Vinyl Gloves Pair/L 71401 - 1 EACH FIRST AID HANDBOOK 72401 – 1 EACH Ice Pack small/boxed EACH 77101 - 1 EACH WIRE SCISSORS 4.5" 77233 - 0.010 ECH Disposable Tweezers 100/bag 805B - STD 0.010 M MF/MFP ASPIRIN BULK

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: e999d2a7-96df-48b9-a0d8-347c7290eb00
Public Version Date: November 06, 2019
Public Version Number: 1
DI Record Publish Date: October 29, 2019