AccessGUDID - DEVICE: alegriaCare (04260505370015)

GUDID

Device Identifier (DI) Information

Brand Name: alegriaCare
Version or Model: 50*50mm
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Wuxi Jiajian Medical Instrument Co.,Ltd.

Primary DI Number: 04260505370015
Issuing Agency: GS1
Commercial Distribution End Date: August 25, 2020
Device Count: 40
Labeler D-U-N-S® Number*: 529966489 *Terms of Use

Device Description: Flexible and easy to fit electrode can be applied to every contour of the human body. You can use the electrodes many times because of its reliable long lasting gel. The unique gel used with the electrode is very cost effective and provides excellent current distribution on the total electrode. Optimal distribution of current . Give patient comfort during stimulation.

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?
61170	Electrical probe/electrode conductive pad	A small, non-sterile device designed to facilitate electrical conduction between an electrical stimulation probe or electrode and the skin. It is typically contoured to fit on a particular type of probe/electrode and is made of an absorbent material (e.g., felt) that may be soaked in a conduction fluid. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
GXY	Electrode, Cutaneous

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: 42fce8db-7302-4137-bb82-5df8e2c780dd
Public Version Date: April 25, 2022
Public Version Number: 3
DI Record Publish Date: August 25, 2017