Moxxly, Inc.

GUDID 00856509007015

MOXXLY, INC.

Breast pump, electric

• Primary Device ID: 00856509007015
• NIH Device Record Key: dc767765-ec0c-4bce-9dc2-de1bf71454c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Moxxly, Inc.
• Version Model Number: Flow Kit (Medium)
• Company DUNS: 079606801
• Company Name: MOXXLY, 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856509007015 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170722

FDA Product Code

• HGX: Pump, Breast, Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-18
• Device Publish Date: 2019-01-16

On-Brand Devices [Moxxly, Inc.]

• 00856509007053: Flow Kit, Valves
• 00856509007046: Flow Kit, Tubing
• 00856509007039: Flow Kit, Bottles
• 00856509007015: Flow Kit (Medium)