microTargeting™ LP+ Electrode Cable 66-EL-LP

GUDID 00873263002582

microTargeting LP+ Patient Lead, Sterile, for use with microTargting Electrodes

FHC, INC.

Depth electrode

• Primary Device ID: 00873263002582
• NIH Device Record Key: 5d200c8f-e25d-4a3f-b0d4-82b3f17ecec5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: microTargeting™ LP+ Electrode Cable
• Version Model Number: 66-EL-LP-00258
• Catalog Number: 66-EL-LP
• Company DUNS: 108179458
• Company Name: FHC, INC.
• Device Count: 1
• 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

Customer Support Contacts

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

Operating and Storage Conditions

• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263002582 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071364

FDA Product Code

• GZL: ELECTRODE, DEPTH

Sterilization

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

[00873263002582]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-09-23
• Device Publish Date: 2016-09-17

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