AccessGUDID - DEVICE: Stainless Steel Facial Ice Globe (00860009308015)

GUDID

Device Identifier (DI) Information

Brand Name: Stainless Steel Facial Ice Globe
Version or Model: Duo Set
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Jiangmen Shengke Hardware Products Co., Ltd

Primary DI Number: 00860009308015
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 402746917 *Terms of Use

Device Description: This ice globe is made of 304 stainless steel and filled with refrigerant. Put it in the refrigerator for 3-4 hours before use, roll it slowly on the face, and enjoy the cool and calm massage effect. It is applicable to the face, neck and other parts.

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:	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?
34661	External manual massager, home-use	A manual (non-powered) device specifically designed to apply external massage in the home. It is typically held in the hand of the user and drawn/rolled across the area of the body/muscles to be treated; it may also be designed to be placed on the floor for foot massage. The massaging components, e.g., roller heads or pads, may be interchangeable with others of different size and shape. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LYG	Massager, Therapeutic, Manual

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: df42ec78-f992-47a2-adc5-01e3d8c7420f
Public Version Date: October 31, 2022
Public Version Number: 1
DI Record Publish Date: October 22, 2022