Genesys HTA Control Unit - Refurbished M00658001R0

GUDID 00850033976021

Genesys HTA 115V Control Unit (Refurbished)

Minerva Surgical, Inc.

Circulating-fluid endometrial-ablation control unit

• Primary Device ID: 00850033976021
• NIH Device Record Key: 2d085379-0507-4d14-b061-86bc8e5d8654
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Genesys HTA Control Unit - Refurbished
• Version Model Number: M00658001R0
• Catalog Number: M00658001R0
• Company DUNS: 829616478
• Company Name: Minerva Surgical, 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com
• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com
• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com
• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com
• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com
• Phone: 855-646-7874
• Email: customerservice@minervasurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850033976021 [Primary]
GS1	08714729809357 [Previous]

FDA Product Code

• MNB: Device, Thermal Ablation, Endometrial

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: 2022-06-16
• Device Publish Date: 2022-06-08

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