Vitrolife

GUDID 07350025912219

Vitrolife Sterile Transmission Gel

NEXT MEDICAL PRODUCTS, LLC

Coupling gel, sterile

• Primary Device ID: 07350025912219
• NIH Device Record Key: d314b060-fba8-46a0-a775-6d5963d70390
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vitrolife
• Version Model Number: 14214
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	07350025912219 [Primary]

FDA Product Code

• IYO: System, Imaging, Pulsed Echo, Ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-25
• Device Publish Date: 2019-04-17

On-Brand Devices [Vitrolife]

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