LithoClear

GUDID 30856724004159

NEXT MEDICAL PRODUCTS, LLC

Coupling gel, non-sterile

• Primary Device ID: 30856724004159
• NIH Device Record Key: 3bbc9696-e5d0-45e3-a410-b0e33a5dcc71
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LithoClear
• Version Model Number: 11-405
• Company DUNS: 078566628
• Company Name: NEXT MEDICAL PRODUCTS, LLC
• Device Count: 4
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10856724004155 [Unit of Use]
GS1	30856724004159 [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: 2018-03-29
• Device Publish Date: 2016-10-24

On-Brand Devices [LithoClear]

• 30856724004159: 11-405
• 30856724004142: 11-601
• 10856724004469: 11-0424
• 10856724004452: LithoClear Gel, High Viscosity, 60 gram