AccessGUDID - DEVICE: High Dens.144 Tip,Fuse (200 Puls), Steril, SubRF (07290109950631)

GUDID

Device Identifier (DI) Information

Brand Name: High Dens.144 Tip,Fuse (200 Puls), Steril, SubRF
Version or Model: AS76694
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: AS76694
Company Name: SYNERON MEDICAL LTD

Primary DI Number: 07290109950631
Issuing Agency: GS1
Commercial Distribution End Date: June 22, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 532685716 *Terms of Use

Device Description: High Dens.144 Tip,Fuse (200 Puls), Steril, SubRF

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:	Yes
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?
45220	Multi-modality skin surface treatment system	An electrically-powered assembly of devices intended to use multiple therapeutic modalities [e.g., intense pulsed light (IPL), laser, radio-frequency (RF) energy, microcurrent electrotherapy, electronic muscle stimulation (EMS), microdermabrasion, hydradermabrasion, oxygen skin application] in combination and/or in isolation for ablative and non-ablative treatment of the skin surface (e.g., removal of pigment/vascular lesions, scarring, acne, psoriasis, wrinkles, tattoos, hair, and skin resurfacing and rejuvenation). The system includes energy/therapy sources (e.g., lasers, lamps, generator) and dedicated applicators (handpieces) intended to apply the different therapies to the skin.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	Electrosurgical, Cutting & Coagulation & Accessories

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: Yes
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: be048195-ddfa-459d-9302-20df65d9a65a
Public Version Date: June 23, 2023
Public Version Number: 5
DI Record Publish Date: September 26, 2016