microTargeting™ Guideline 4000 LP+™ Breakout Box MT-LPP-BOX

GUDID 00873263002797

microTargeting Guideline 4000 LP+ Breakout Box

FHC, INC.

Neurophysiologic monitoring system

• Primary Device ID: 00873263002797
• NIH Device Record Key: 985370f0-6e5a-4bfd-bcd4-4008d03c2fec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: microTargeting™ Guideline 4000 LP+™ Breakout Box
• Version Model Number: MT-LPP-BOX-00279
• Catalog Number: MT-LPP-BOX
• 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: 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

Customer Support Contacts

• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com

Operating and Storage Conditions

• Storage Environment Atmospheric Pressure: Between 50 KiloPascal and 106 KiloPascal
• Storage Environment Atmospheric Pressure: Between 50 KiloPascal and 106 KiloPascal
• Storage Environment Atmospheric Pressure: Between 50 KiloPascal and 106 KiloPascal
• Storage Environment Atmospheric Pressure: Between 50 KiloPascal and 106 KiloPascal

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263002797 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071364

FDA Product Code

• GZL: ELECTRODE, DEPTH

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-17

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