Liberty

GUDID 10840861102713

Liberty Cycler Set, single stay•safe® PIN patient connector, 15-foot drain line – integrated set

Fresenius Medical Care Renal Therapies Group, LLC

Peritoneal dialysis system tubing set

• Primary Device ID: 10840861102713
• NIH Device Record Key: 5af7b8bf-adbf-41d5-995b-588164014ffa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liberty
• Version Model Number: 050-87216A
• Company DUNS: 079732391
• Company Name: Fresenius Medical Care Renal Therapies Group, LLC
• 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: true
• 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)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx
• Phone: 1(800)323-5188
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840861102716 [Primary]
GS1	10840861102713 [Package]; Contains: 00840861102716; Package: Case [14 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173718

FDA Product Code

• FKX: System, Peritoneal, Automatic Delivery

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: 2024-03-27
• Device Publish Date: 2024-03-19

On-Brand Devices [Liberty]

• 10840861102713: Liberty Cycler Set, single stay•safe® PIN patient connector, 15-foot drain line – integrate
• 10840861102706: Liberty Cycler Set, single stay•safe® PIN patient connector, 10-foot patient line, 30-inch dr