Vertek

GUDID 00763000581244

VERTEK 9733936 PASSIVE BIOPSY KIT

MEDTRONIC NAVIGATION, INC.

Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system Neurological stereotactic surgery system

• Primary Device ID: 00763000581244
• NIH Device Record Key: cf8186f2-74ce-419a-abb4-75dd401f5167
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000581244 [Primary]

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

[00763000581244]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-19
• Device Publish Date: 2022-08-11

On-Brand Devices [Vertek]

• 00763000662271: VERTEK 9733936 PASSIVE BIOPSY KIT
• 00763000581244: VERTEK 9733936 PASSIVE BIOPSY KIT