vPad2 Connector Cable INS-0048

GUDID 00815686020392

VERAN MEDICAL TECHNOLOGIES INC.

Electromagnetic device tracking system fiducial marker Electromagnetic device tracking system fiducial marker Electromagnetic device tracking system fiducial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker Electromagnetic device tracking system spatial marker

• Primary Device ID: 00815686020392
• NIH Device Record Key: c060cefc-1883-4c14-92f4-4fce8c12270c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: vPad2 Connector Cable
• Version Model Number: INS-0048
• Catalog Number: INS-0048
• Company DUNS: 181714804
• Company Name: VERAN MEDICAL TECHNOLOGIES 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: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815686020392 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122106

FDA Product Code

• JAK: System, X-Ray, Tomography, Computed

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: 2016-08-31

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