RF CONDUCTR™ MC

GUDID 00643169148048

CATH 07856042 RF CONDUCTR W/O CE

MEDTRONIC, INC.

Cardiac radio-frequency ablation system catheter

• Primary Device ID: 00643169148048
• NIH Device Record Key: 1fb6b922-2a5d-4233-bfa6-65370c20cb4e
• Commercial Distribution Discontinuation: 2018-11-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RF CONDUCTR™ MC
• Version Model Number: 07856042
• 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: true
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169148048 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P930029

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-18
• Device Publish Date: 2014-09-23

On-Brand Devices [RF CONDUCTR™ MC]

• 00643169148161: CATH 0787533 RF CONDUCTR W/O CE
• 00643169148147: CATH 0786044 RF CONDUCTR W/O CE
• 00643169148123: CATH 0786042 RF CONDUCTR W/O CE
• 00643169148109: CATH 0786022 RF CONDUCTR W/O CE
• 00643169148086: CATH 07857544 RF CONDUCTR W/O CE
• 00643169148062: CATH 07856044 RF CONDUCTR W/O CE
• 00643169148048: CATH 07856042 RF CONDUCTR W/O CE
• 00643169147805: CATH 0787544 RF CONDUCTR W/O CE
• 00763000227838: CATH 0786042 RF CONDUCTR MC W/O CE
• 00763000227814: CATH 0787533 RF CONDUCTR MC W/O CE