GUDID 00643169913004

REDUCING TUBE 9735733 3.2MM CRANIAL

MEDTRONIC NAVIGATION, INC.

Neurological stereotactic surgery system

• Primary Device ID: 00643169913004
• NIH Device Record Key: 9518e4a1-4451-45a8-953a-80a874351371
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9735733
• Company DUNS: 835233107
• Company Name: MEDTRONIC NAVIGATION, 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: 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)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Lumen/Inner Diameter: 3.2 Millimeter
• Lumen/Inner Diameter: 3.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169913004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162604

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00643169913004]

Moist Heat or Steam Sterilization

[00643169913004]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-02-11

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