AccessGUDID - DEVICE: WINNER EVO PACKAGE (00852515007193)

GUDID

Device Identifier (DI) Information

Brand Name: WINNER EVO PACKAGE
Version or Model: 410-016-220
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: COMPASS HEALTH BRANDS CORP.

Primary DI Number: 00852515007193
Issuing Agency: GS1
Commercial Distribution End Date: October 31, 2018
Device Count: 1
Labeler D-U-N-S® Number*: 827221698 *Terms of Use

Device Description: ST4 220, 2X2 MS FOAM, LASER MODULE, LEAD CORDS

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):	No
Kit:	No
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?
35995	Transcutaneous electrical stimulation electrode, single-use	An electrical conductor intended to be attached to a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle stimulation (EMS), cranial electrotherapy stimulation (CES)]. It is typically a flat, flexible, conductive pad with an adhesive (e.g., gel), or a preformed shape/mechanism designed for attachment to a particular body part (e.g., earclip), connected to a conductive wire. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
ILY	Lamp, Infrared, Therapeutic Heating
GXY	Electrode, Cutaneous
LIH	Interferential Current Therapy
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief
IFP	Formalin, Neutral Buffered

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: 630dae55-0b06-454e-b414-426b9c80b55f
Public Version Date: August 29, 2023
Public Version Number: 7
DI Record Publish Date: November 21, 2016