AccessGUDID - DEVICE: BE SMART GET PREPARED (00020424021429)

GUDID

Device Identifier (DI) Information

Brand Name: BE SMART GET PREPARED
Version or Model: 10OUT02142; 10OUT02142REV1
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: TOTAL RESOURCES INTERNATIONAL INC.

Primary DI Number: 00020424021429
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 790160535 *Terms of Use

Device Description: Are We There Yet? Travel Essentials by Be Smart Get Prepared, 84 Pieces – PPE, Camping, Hiking, Fishing, Boating, Family - (9) Alcohol Prep Pads; (9) Antiseptic Wipes; (3) Hand Sanitizers 0.05 oz; (3) Antibiotic Ointments; (20) Sheer Bandages 1 in x 3 in; (15) Sheer Bandages 5/8 in x 2 1/4 in; (10) Toilet Seat Covers; (2) Deodorant Gels 0.12 oz; (1) Toilet Paper; (1) Flushable Wet Wipe; (1) Body Wipe 12 in x 12 in; (6) Examination Gloves 3 pairs; (3) Face Masks; (1) First Aid Guide English & Spanish

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):	Yes
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:	No
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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f3dbfe2f-3aa5-4c0b-b16d-912109fe85db
Public Version Date: January 08, 2025
Public Version Number: 2
DI Record Publish Date: January 05, 2024