Primary Device ID | 00869851000399 |
NIH Device Record Key | 240e93ae-b813-45a0-9d0f-67f5e165dfd7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FiLaC |
Version Model Number | 101260 |
Catalog Number | 101260 |
Company DUNS | 080537625 |
Company Name | WISDOM MEDICAL TECHNOLOGY, LLC |
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 | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net | |
Phone | 630-803-6383 |
jfurcht@verizon.net |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00869851000399 [Primary] |
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 | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-09-05 |
00859337007158 - MegaBeam | 2023-06-02 lateral emitting laser fiber, single use, 600 micron radial tip |
00859337007165 - MegaBeam | 2023-06-02 lateral emitting laser fiber, single use, 400 micron, radial tip |
00859337007141 - Twister L | 2021-04-08 lateral emitting laser fiber |
00859337007134 - MegaBeam | 2020-12-08 end emitting laser fiber, single use, 600 micron, SF |
00859337007127 - MegaBeam | 2020-10-07 end emitting laser fiber, single use, 600 micron flat tip |
00859337007110 - MegaBeam | 2019-11-12 MegaBeam® Single Use, Handpiece |
00859337007080 - MegaBeam | 2019-03-04 Twister 600um SMA, side firing laser fiber, single use |
00859337007103 - Twister | 2018-10-29 lateral emitting laser fiber |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FILAC 85439167 4645460 Live/Registered |
BIOLITEC UNTERNEHMENSBETEILIGUNGS II AG 2011-10-04 |
FILAC 73763346 1548995 Live/Registered |
SHERWOOD MEDICAL COMPANY 1988-11-14 |