AccessGUDID - DEVICE: Bleeding Control Kit Plus 6/cs (M689WJBBC4010)

GUDID

Device Identifier (DI) Information

Brand Name: Bleeding Control Kit Plus 6/cs
Version or Model: 01
Commercial Distribution Status: In Commercial Distribution
Catalog Number: WJBBC4
Company Name: Safeguard US Operating, LLC

Primary DI Number: M689WJBBC4010
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 118492643 *Terms of Use

Device Description: The Bleeding Control Kit Plus 6/cs is apart of the Public Access Trauma Kits are vacuum sealed kits that include instructions and interventions to address immediate threats to life from massive hemorrhage, airway compromise, respiratory, lacerations and hypothermia. This kit is designed to treat one to three persons dependent on severity and distribution of injuries.

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:	Yes
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?
44047	First aid kit, non-medicated, single-use	A convenient collection of equipment and materials intended to be used in an emergency for the rapid, initial treatment of an injury. This device is typically used by emergency medical services (EMS), institutions, schools, the home, motor vehicles, and other public settings. This device does not contain medicinal substances/pharmaceuticals. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OHO	First Aid Kit Without 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: 5d82e2b8-5fcf-46cd-88ae-782641611ee6
Public Version Date: April 10, 2026
Public Version Number: 1
DI Record Publish Date: April 02, 2026