Double Pump Kit, Willow Go

GUDID 00810104130486

Double Pump Kit, Willow Go (Lucy)

EXPLORAMED NC7, INC.

Breast pump, electric

• Primary Device ID: 00810104130486
• NIH Device Record Key: 53634413-7f80-4b83-bd93-6f270e384a97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Double Pump Kit, Willow Go
• Version Model Number: CPDL90
• Company DUNS: 050917861
• Company Name: EXPLORAMED NC7, 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: false
• Lot Batch: false
• Serial Number: true
• 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	00810104130486 [Primary]

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: 2023-04-20
• Device Publish Date: 2023-04-12

On-Brand Devices [Double Pump Kit, Willow Go]

• 00858298006583: Double Pump Kit, Willow Go (Lucy)
• 00810104130486: Double Pump Kit, Willow Go (Lucy)