Vitrolife

GUDID 07350025911205

Vitrolife Ultrasound Transmission Gel

NEXT MEDICAL PRODUCTS, LLC

Topical coupling gel, non-sterile

• Primary Device ID: 07350025911205
• NIH Device Record Key: c04e0624-fd1a-45f1-b5fc-1ea173a5d12e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vitrolife
• Version Model Number: 14213
• Company DUNS: 078566628
• Company Name: NEXT MEDICAL PRODUCTS, LLC
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350025911205 [Primary]

FDA Product Code

• IYO: System, Imaging, Pulsed Echo, Ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-06-10
• Device Publish Date: 2020-10-05

On-Brand Devices [Vitrolife]

• 07350025912219: Vitrolife Sterile Transmission Gel
• 07350025911212: Vitrolife Ultrasound Transmission Gel
• 07350025911205: Vitrolife Ultrasound Transmission Gel