Willow Go Replacement Pump

GUDID 00858298006620

Willow Go Replacement Pump

EXPLORAMED NC7, INC.

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• Primary Device ID: 00858298006620
• NIH Device Record Key: 09eda263-6b65-43c5-94f3-03ab93f96694
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Willow Go Replacement Pump
• Version Model Number: PDL61
• 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	00858298006620 [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: 2022-09-08
• Device Publish Date: 2022-08-31

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