ClosureRFS™

GUDID 00763000723293

STYLET RFS2-6-12 CLOSUREFAST

MEDTRONIC, INC.

Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter Peripheral vascular radio-frequency ablation catheter

• Primary Device ID: 00763000723293
• NIH Device Record Key: 1ec809b6-f276-430b-878b-6457b45d4696
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ClosureRFS™
• Version Model Number: RFS2-6-12
• 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: false
• 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
• 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 Dimensions

• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter
• Device Size Text, specify: 0
• Length: 12 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry area away from sunlight.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000723293 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052003

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-27
• Device Publish Date: 2024-05-19

On-Brand Devices [ClosureRFS™]

• 00643169862999: STYLET RFS2-6-12 CLOSURE FAST V02
• 00763000723293: STYLET RFS2-6-12 CLOSUREFAST