Primary Device ID | 00873263007815 |
NIH Device Record Key | fddbb809-7da0-4920-9818-77a8a0e070dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | microTargeting™ Electrode Lead Cable |
Version Model Number | C0232-00781 |
Catalog Number | C0232 |
Company DUNS | 108179458 |
Company Name | FHC, 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 | 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 | +1(800)326-2905 |
fhcinc@fh-co.com |
Length | 1.5 Meter |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00873263007815 [Primary] |
GZL | ELECTRODE, DEPTH |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00873263007815]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2019-07-30 |
00873263006917 | GL5 UE Patient Lead, 1.5m, presterile |
00873263006900 | GL5 UE Patient Lead, 3m, presterile |
00873263007815 | Guidline 4000 ™ 5.0 1.5m Special-use Lead, 1x For use with microTargeting ™ Electrodes |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROTARGETING 78392262 not registered Dead/Abandoned |
TargetPoint Consulting, Inc 2004-03-29 |
MICROTARGETING 76709829 4259360 Dead/Cancelled |
Siren Interactive Corp. 2011-11-23 |
MICROTARGETING 74600530 1921303 Dead/Cancelled |
MBV, INC. 1994-11-18 |