microTargeting Insertion Tube 66-IT-AR4P

GUDID 10873263003494

microTargeting Lead Insertion Tube with Stylet, Sterile, for use with microTargeting Platform

FHC, INC.

Intracerebral cannula, implantable
Primary Device ID10873263003494
NIH Device Record Key195a4ff8-3a0e-441b-bd82-6127eb9451e5
Commercial Distribution StatusIn Commercial Distribution
Brand NamemicroTargeting Insertion Tube
Version Model Number66-IT-AR4P-00349
Catalog Number66-IT-AR4P
Company DUNS108179458
Company NameFHC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)326-2905
Emailfhcinc@fh-co.com

Device Dimensions

Outer Diameter1.83 Millimeter
Outer Diameter1.83 Millimeter
Outer Diameter1.83 Millimeter

Operating and Storage Conditions

Handling Environment HumidityBetween 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Handling Environment HumidityBetween 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Handling Environment HumidityBetween 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
GS100873263003497 [Primary]
GS110873263003494 [Package]
Contains: 00873263003497
Package: PK/5 [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HAWNeurological stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10873263003494]

Ethylene Oxide;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-17

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