Vertek®

GUDID 00763000223113

VERTEK 9733936 PASSIVE BIOPSY KIT

MEDTRONIC NAVIGATION, INC.

Neurological stereotactic surgery system

• Primary Device ID: 00763000223113
• NIH Device Record Key: 8f3574ba-8931-4435-bf99-3361ce7460f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vertek®
• Version Model Number: 9733936
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000223113 [Primary]

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00763000223113]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-05
• Device Publish Date: 2019-02-02

On-Brand Devices [Vertek®]

• 00613994467522: VERTEK 9733936 PASSIVE BIOPSY KIT
• 00613994285652: UPGRADE KIT 9733266 VERTEK, PASSIVE BIOP
• 00763000201234: VERTEK UPGRADE KIT 9733266 PASS BIOP
• 00763000251741: VERTEK 9733936 PASSIVE BIOPSY KIT
• 00763000234744: VERKEK UPGRADE KIT 9733266 PASS BIOP
• 00763000223113: VERTEK 9733936 PASSIVE BIOPSY KIT
• 00763000167974: VERTEK 9733936 PASSIVE BIOPSY KIT
• 00763000927202: VERTEK 9733936 PASSIVE BIOPSY KIT