Primary Device ID | 00816722021618 |
NIH Device Record Key | f65c1986-08cf-49bc-a8df-0a7ebe2c24d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | enlighten |
Version Model Number | enlighten Low Energy Green |
Company DUNS | 041071643 |
Company Name | CUTERA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com | |
Phone | 1 415 657-5500 |
info@cutera.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816722021618 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-23 |
00816722023605 | enlighten Micro Lens Array handpiece attachment |
00816722021649 | enlighten III Laser System |
00816722021625 | enlighten SR Laser System |
00816722021618 | enlighten Low Energy Green Laser System |
00816722021601 | enlighten Laser System |