Safe-Lock®

GUDID 00840861100705

Safe-Lock® Catheter Adapter Co-Pack Type II

Fresenius Medical Care Holdings, Inc.

Peritoneal dialysis catheter adaptor, single-use

• Primary Device ID: 00840861100705
• NIH Device Record Key: dd6f465c-cc5c-4d88-887f-fdbd7006728b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safe-Lock®
• Version Model Number: 050-75000
• Company DUNS: 958291411
• Company Name: Fresenius Medical Care Holdings, 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)323-5188
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840861100705 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K822550

FDA Product Code

• FKX: SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-02

On-Brand Devices [Safe-Lock®]

• 10840861100818: APD Luer-Lock Adapter
• 00840861100705: Safe-Lock® Catheter Adapter Co-Pack Type II
• 10840861100665: Safe-Lock® Universal Connector
• 10840861100658: Safe-Lock® Catheter Adapter Sealing Cap