AccessGUDID - DEVICE: Cramer Sports Medicine Junior Soft-Sided Athletic Trainer's Kit

GUDID

Device Identifier (DI) Information

Brand Name: Cramer Sports Medicine Junior Soft-Sided Athletic Trainer's Kit - Equipped
Version or Model: 121800
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: CRAMER PRODUCTS, INC.

Primary DI Number: 00311960640817
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 007138183 *Terms of Use

Device Description: Junior Soft-Sided Athletic Trainer's Kit - Equipped 1Tuf-Tek Junior Soft Sided Empty, (1) 3" Elastic Wrap , (1) Tuf-Skin, (1) PVP Pack , (1) Roll Athletic Tape , (1) Instant Cold Pack , (2) Latex Gloves , (1) Bulk Bandage Pack , (1) Skin Lube , (1) Sam Finger Splint , (1) Iso-Quin, (1) Sports Injury Handbook , (1) Zip-Cut, (1) Atomic Balm, (1) Cinder Suds, (1) Tape Underwrap , (1) Pocket Mirror , (1) Sterile Eye Wash , (10) Antibiotic Creams

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:	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
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: 365e5de1-f10c-40e8-a914-4432c55af9cd
Public Version Date: May 01, 2019
Public Version Number: 1
DI Record Publish Date: April 23, 2019