Guideline 4000 5.0™ microTargeting™ Interface Card C0218

GUDID 00873263006801

Guideline 4000 5.0(TM) microTargeting(TM) Interface Card

FHC, INC.

Neurophysiologic monitoring system
Primary Device ID00873263006801
NIH Device Record Keye462eaa3-0f28-4de8-a67d-7a4071321d0b
Commercial Distribution StatusIn Commercial Distribution
Brand NameGuideline 4000 5.0™ microTargeting™ Interface Card
Version Model NumberC0218-00680
Catalog NumberC0218
Company DUNS108179458
Company NameFHC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100873263006801 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZLELECTRODE, DEPTH

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-02-04
Device Publish Date2019-01-02

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