CMExpress® Set with Needleless Y Sites

GUDID 10818666020327

80 in. (200 cm) Microbore Set - Blue Stripe, Spike with Drip Chamber For Use with the CMExpress® Infusion Pump

CME AMERICA LLC

Electric infusion pump administration set, single-use

• Primary Device ID: 10818666020327
• NIH Device Record Key: 6562a9c5-c3b9-4fab-ab0c-b7eef436dd93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CMExpress® Set with Needleless Y Sites
• Version Model Number: A120-160CYFRV
• Company DUNS: 002125419
• Company Name: CME AMERICA 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx
• Phone: 303-936-4945
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00818666020320 [Primary]
GS1	10818666020327 [Package]; Contains: 00818666020320; Package: Case [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042696

FDA Product Code

• FPA: Set, Administration, Intravascular

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: 2017-06-16

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• B101100100POBSC0 - T34 Syringe Pump System: 2018-12-03 Pump, Operator's Manual
• B101100100PSA0 - T34 Syringe Pump System: 2018-12-03 Pump, Operator's Manual
• B101100100PSLA0 - T34L Syringe Pump System: 2018-12-03 Pump, wall charger, operations manual
• B101100100SA0 - T34 Syringe Pump: 2018-12-03
• B101100100SLA0 - T34L Syringe Pump: 2018-12-03