Primary Device ID | 00873263003503 |
NIH Device Record Key | 5904e18a-6df2-4c12-9e45-af5f4edd36ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | microTargeting™ Drive System |
Version Model Number | MT-DS-01-00350 |
Catalog Number | MT-DS-01 |
Company DUNS | 108179458 |
Company Name | FHC, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
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 | +1(800)326-2905 |
fhcinc@fh-co.com |
Storage Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00873263003503 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00873263003503]
Hydrogen Peroxide;Moist Heat or Steam Sterilization;Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-17 |
00873263003527 | microTargeting Drive System Contains: -microTargeting Manual Drive -Drive Mount and Guide -micro |
00873263003503 | microTargeting(TM) Drive System compatible with mT Controller Contains: - Verification Probe - m |
00873263001479 | microTargeting Drive System |
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 |