Novaplus

GUDID 20856724004503

Novaplus Singles, High Viscosity

NEXT MEDICAL PRODUCTS, LLC

Skin topical coupling gel

• Primary Device ID: 20856724004503
• NIH Device Record Key: cfb197be-d62a-4b89-893c-61b1993b2ee2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Novaplus
• Version Model Number: V02-400B-030
• 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: true
• 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	20856724004503 [Unit of Use]
GS1	30856724004500 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-20
• Device Publish Date: 2023-06-12

On-Brand Devices [Novaplus]

• 10856724004551: V06-400-030
• 20856724004527: Novaplus Singles, High Viscosity
• 20856724004503: Novaplus Singles, High Viscosity
• 10856724004490: Novaplus Ultrasound Gel, Medium Viscosity, 8 oz.
• 10856724004483: Novaplus Ultrasound Gel, High Viscosity, 8 oz. bottle