ClosureFast™

GUDID 00643169862968

CATHETER CF7-7-60 CLOSURE FAST V03

MEDTRONIC, INC.

Peripheral vascular electrocautery catheter, single-use Peripheral vascular electrocautery catheter, single-use

• Primary Device ID: 00643169862968
• NIH Device Record Key: 78d88304-c515-4464-a6d3-93bb8f2fd567
• Commercial Distribution Discontinuation: 2018-07-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ClosureFast™
• Version Model Number: CF7-7-60
• 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

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 15 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169862968 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061373

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

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: 2019-03-11
• Device Publish Date: 2017-05-14

On-Brand Devices [ClosureFast™]

• 00643169862982: CATHETER CF7-7-100 CLOSURE FAST V03
• 00643169862975: CATHETER CF7-7-100 CLOSURE FAST V02
• 00643169862968: CATHETER CF7-7-60 CLOSURE FAST V03
• 00643169862951: CATHETER CF7-7-60 CLOSURE FAST V02
• 00643169862944: CATHETER CF7-3-60 CLOSURE FAST V03
• 00643169862937: CATHETER CF7-3-60 CLOSURE FAST V02
• 00763000022273: Catheter CF7-7-60 Closure Fast V04
• 00763000552176: CATHETER CF6-8-100 CLOSUREFAST
• 00763000552169: CATHETER CF6-8-60 CLOSUREFAST
• 00763000702298: CATHETER CF7-3-60 CLOSURE FAST V05
• 00763000702281: CATHETER CF7-7-60 CLOSURE FAST V05
• 00763000702274: CATHETER CF7-7-100 CLOSURE FAST V05