IMACTIS®

GUDID B681A102001

Non-sterile needle holder of the IMACTIS® CT-NAVIGATION system

IMACTIS

Electromagnetic surgical navigation device tracking system

• Primary Device ID: B681A102001
• NIH Device Record Key: 876f83df-f171-4f96-afd6-46e180b92f92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMACTIS®
• Version Model Number: A10200
• Company DUNS: 260527568
• Company Name: IMACTIS
• 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: false
• Lot Batch: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B681A102001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162314

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-01-07
• Device Publish Date: 2018-12-07

On-Brand Devices [IMACTIS® ]

• B681J020000: Navigation station of the IMACTIS® CT-NAVIGATION system
• B681J001971: Transport suitcase for the navigation station of the IMACTIS® CT-NAVIGATION system
• B681J00099US0: Power cable of the IMACTIS® CT-NAVIGATION system
• B681J000970: Cart for the IMACTIS® CT-NAVIGATION system
• B681I101002: Single use Navigation Kit of the IMACTIS® CT-NAVIGATION system
• B681A102001: Non-sterile needle holder of the IMACTIS® CT-NAVIGATION system
• B681A100101: Sterile needle holder of the IMACTIS® CT-NAVIGATION system