BodyGuard® MicroSet with Needleless Adapters

GUDID 10818666020358

63 in. (159 cm) MicroSet with Needleless Y Sites For Use with the BodyGuard® Infusion Pump

CME AMERICA LLC

Electric infusion pump administration set, single-use

• Primary Device ID: 10818666020358
• NIH Device Record Key: a559e6bf-82b4-4377-9e12-1e58cd01b2ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BodyGuard® MicroSet with Needleless Adapters
• Version Model Number: A120-160X2YB
• 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	00818666020351 [Primary]
GS1	10818666020358 [Package]; Contains: 00818666020351; 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: 2017-06-21

On-Brand Devices [BodyGuard® MicroSet with Needleless Adapters]

• 10818666020358: 63 in. (159 cm) MicroSet with Needleless Y Sites For Use with the BodyGuard® Infusion Pump
• B101A120160X2YB1: 63 in. (159 cm) MicroSet with Needleless Y Sites For Use with the BodyGuard® Infusion Pump