GUDID 00643169946644

CONSOLE 106A3 GENV US PLEXUS ROHS

MEDTRONIC, INC.

Cardiac cryosurgical system

• Primary Device ID: 00643169946644
• NIH Device Record Key: 981886d9-9f55-4826-bde3-f939388c66ca
• Commercial Distribution Discontinuation: 2018-10-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 106A3
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• Serial Number: true
• 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

Operating and Storage Conditions

• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169946644 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P020045

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-13
• Device Publish Date: 2017-02-20

Devices Manufactured by MEDTRONIC, INC.

• 00199150057177 - NA: 2025-11-24 CUSTOM PACK BB3Z71R34 HLO PRIMARY
• 00199150058976 - NA: 2025-11-24 CUSTOM PACK PDBB12P71R2 HLO HEATT
• 00199150060122 - NA: 2025-11-24 CUSTOM PACK BB12S52R1 EVL 3/8 PACK
• 00763000849801 - Liberant™: 2025-11-24 CONSOLE LMT-BCU LIBERANT
• 00763000913069 - InterStim™ SureScan™: 2025-11-24 LEAD 978A128 ISTM 2.16MM EUMDR EMAN LI08
• 00763000913083 - InterStim™ SureScan™: 2025-11-24 LEAD 978A133 ISTM 2.16MM EMAN EUMDR LI08
• 00763000913106 - InterStim™ SureScan™: 2025-11-24 LEAD 978A141 ISTM 2.16MM EMAN EUMDR LI08
• 00763000913120 - InterStim™ SureScan™: 2025-11-24 LEAD 978B128 ISTM 4.32MM EUMDR EMAN LI08