Primary Device ID | 10873263007539 |
NIH Device Record Key | 7dd5bc1d-b058-42b8-a07e-b5b518d6bad5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | microTargeting™ Electrode and Insertion Tube |
Version Model Number | FC4000-00753 |
Catalog Number | FC4000 |
Company DUNS | 108179458 |
Company Name | FHC, INC. |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00873263007532 [Unit of Use] |
GS1 | 10873263007539 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10873263007539]
Ethylene Oxide;Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-06 |
Device Publish Date | 2019-12-27 |
10873263001155 | microTargeting single electrode insertion tubes and electrodes kit, 5x, Sterile for use with Nex |
10873263007539 | microTargeting single electrode insertion tubes and electrodes kit, 5x, Sterile for use with Nex |
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 |