Primary Device ID | 07290109142401 |
NIH Device Record Key | 8d09e1df-2a5a-4698-a071-1a44422b5c6e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SurgiTouch™ Scanner |
Version Model Number | Upgrade kit for AcuPulse 30/40 ST |
Company DUNS | 600166524 |
Company Name | LUMENIS LTD. |
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 | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx | |
Phone | 408-764-3000 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109142401 [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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-07 |
07290109142975 | SurgiTouch™ Scanner |
07290109142401 | Upgrade kit for AcuPulse 30/40 ST |
07290109142203 | kit for AcuPulse and AcuPulse DUO |
07290109142135 | Kit for UltraPulse SurgiTouch |
07290109142111 | kit for UltraPulse/UltraPulse DUO |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURGITOUCH 73792163 1628168 Dead/Cancelled |
HO DENTAL COMPANY, INC. 1989-04-10 |