PoleStar®

GUDID 00885074370064

POLESTAR, 9731357, PASSIVE PLANAR-BRONZE

MEDTRONIC NAVIGATION, INC.

Stereotactic surgery system probe, reusable

• Primary Device ID: 00885074370064
• NIH Device Record Key: d652bced-4d09-40a8-a49a-b863e44750aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PoleStar®
• Version Model Number: 9731357
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00885074370064 [Primary]

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00885074370064]

Moist Heat or Steam Sterilization

[00885074370064]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-18

On-Brand Devices [PoleStar®]

• 00613994209658: FLEXCOIL 9733063 BAND D/E ADJUSTBLE 10PK
• 00643169351721: INST SET 9733999 POLESTAR
• 00885074370064: POLESTAR, 9731357, PASSIVE PLANAR-BRONZE
• 00885074361529: FRAME, 9731724, DETACH PASSIVE PATIENT