Primary Device ID | 07290109140537 |
NIH Device Record Key | 305ee98b-f954-49ea-80e8-af24cf12c62e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lumenis Pulse 50H |
Version Model Number | Lumenis Pulse 50H |
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 | 07290109140537 [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 | 2016-08-23 |
07290109140537 | Lumenis Pulse 50H |
07290109145976 | Lumenis Pulse 50H |
07290109147277 | Lumenis Pulse 50H |
07290109147253 | Lumenis Pulse 50H |