Primary Device ID | 17290109140169 |
NIH Device Record Key | 9e7d0673-90eb-4646-bed3-2d1e15ac0a96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Slimline EZ 200 Fiber |
Version Model Number | Slimline EZ 200 Fiber |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109140162 [Primary] |
GS1 | 17290109140169 [Package] Contains: 07290109140162 Package: [3 Units] In Commercial Distribution |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-21 |
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