BodyGuard® Microset with Needleless Y-Site

GUDID 10818666020143

150 in. (380 cm) For Use with the BodyGuard® Infusion Pump

CME AMERICA LLC

Electric infusion pump administration set, single-use

• Primary Device ID: 10818666020143
• NIH Device Record Key: 1d70f0bf-e268-431e-8522-57e0508d84a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BodyGuard® Microset with Needleless Y-Site
• Version Model Number: A120-003XYVA
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00818666020146 [Primary]
GS1	10818666020143 [Package]; Contains: 00818666020146; 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: 2017-06-15

On-Brand Devices [BodyGuard® Microset with Needleless Y-Site]

• 10818666020143: 150 in. (380 cm) For Use with the BodyGuard® Infusion Pump
• B101A120003XYVA0: 150 in. (380 cm) For Use with the BodyGuard® Infusion Pump