Autoguide

GUDID 00763000573720

REDUCING TUBE 9736381 2.5MM SEEG

MEDTRONIC NAVIGATION, INC.

Brain biopsy procedure kit

• Primary Device ID: 00763000573720
• NIH Device Record Key: 055c98be-9a46-4ee3-806c-05fe3bafdb22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Autoguide
• Version Model Number: 9736381
• 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: true
• 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
• 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	00763000573720 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191597

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

[00763000573720]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-11
• Device Publish Date: 2022-04-02

On-Brand Devices [Autoguide]

• 00763000536329: STAB INCISION HGT GUIDE 27563 AUTOGUIDE
• 00763000573720: REDUCING TUBE 9736381 2.5MM SEEG
• 00763000573713: DRILL GUIDE 9736380 BLUNT AUTOGUIDE