AccessGUDID - DEVICE: SUPERCHARGE HYDRA FASCIA ELECTRODES (08056182721167)

GUDID

Device Identifier (DI) Information

Brand Name: SUPERCHARGE HYDRA FASCIA ELECTRODES
Version or Model: Lymphanova oval Ømaj 60mm
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 17730
Company Name: UNIBELL SRL

Primary DI Number: 08056182721167
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 338736462 *Terms of Use

Device Description: Lymphanova oval Ømaj 60mm, thickness 14 mm, is a capacitive electrode designed specifically for the HCR1002 medical device.

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):	Yes
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?
47575	Medium-wave diathermy treatment system	An assembly of devices designed to produce a therapeutic deep heat within specific volumes of the body through the transcutaneous transmission of electromagnetic (EM) energy in the radio-frequency (RF) bands of 0.5 megahertz (MHz) to 1 MHz. It typically consists of an electric generator and two electrodes (active and return) intended to be held on/near the patient. The system is commonly used in outpatient, rehabilitation, traumatology, and sports centre settings to treat pain, muscle spasms, and joint contractures; it is not used for surgery or to treat malignancies.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PBX	Massager, Vacuum, Radio Frequency Induced Heat

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K181211	000

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: 9b895d11-446b-474e-a1e6-f75be53d3120
Public Version Date: March 24, 2026
Public Version Number: 1
DI Record Publish Date: March 16, 2026