Primary Device ID | 07290109143392 |
NIH Device Record Key | 5d50a984-1776-4d38-940d-2209448fb7c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LaserLink Z |
Version Model Number | LaserLink Z |
Company DUNS | 043618763 |
Company Name | LUMENIS 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 | 408-764-3000 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109143392 [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 | 2016-08-31 |
07290109143668 | LaserLink Z |
07290109143392 | LaserLink Z |
07290109143385 | LaserLink Z |