MINIMAX Minimally Invasive Retractor MMX-1

GUDID B040MMX1

Multipurpose retractor for minimally invasive thoracic use

GENESEE BIOMEDICAL, INC.

Sternum spreader

• Primary Device ID: B040MMX1
• NIH Device Record Key: 9d32b744-8ca0-4dff-9318-6a130dc8a75f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MINIMAX Minimally Invasive Retractor
• Version Model Number: MMX-1
• Catalog Number: MMX-1
• Company DUNS: 939872651
• Company Name: GENESEE BIOMEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com
• Phone: 800-786-4980
• Email: contact@geneseebiomedical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B040MMX1 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

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

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

[B040MMX1]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-09-05
• Device Publish Date: 2024-08-28

On-Brand Devices [MINIMAX Minimally Invasive Retractor ]

• BO40MMX1RS0: Multipurpose retractor for minimally invasive thoracic use including both radiolucent and stainl
• B040MMX1R0: Multipurpose retractor for minimally invasive thoracic use including radiolucent blades
• B040MMX1: Multipurpose retractor for minimally invasive thoracic use