omniTRAX Patient Tracker Starter Kit H4913AT

GUDID 00841436109406

Reusable non-sterile multi-modality fiducial markers (5), reusable non-sterile general purpose electromagnetic sensor for use with 3D Guidance driveBAY™, driveBAY™ 2, trakSTAR™ or trakSTAR™ 2 trackers

CIVCO MEDICAL INSTRUMENTS CO., INC.

Electromagnetic device tracking system fiducial marker

• Primary Device ID: 00841436109406
• NIH Device Record Key: 8d8c1401-fdb5-4020-812f-54efcad313bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: omniTRAX Patient Tracker Starter Kit
• Version Model Number: H4913AT
• Catalog Number: H4913AT
• Company DUNS: 134614411
• Company Name: CIVCO MEDICAL INSTRUMENTS CO., 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com

Device Dimensions

• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch
• Width: 7 Inch
• Length: 1.95 Inch

Operating and Storage Conditions

• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841436109406 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092619

FDA Product Code

• IYO: System, imaging, pulsed echo, ultrasonic

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: 2017-08-22

On-Brand Devices [omniTRAX Patient Tracker Starter Kit]

• 00841436109406: Reusable non-sterile multi-modality fiducial markers (5), reusable non-sterile general purpose e
• 00841436102636: Reusable non-sterile multi-modality fiducial markers (5), reusable non-sterile general purpose e
• 00841436101042: Reusable non-sterile multi-modality fiducial markers (5), reusable non-sterile general purpose e