Nutrifill

GUDID 00850012123019

Ultra-Pure Nutrient Rich Specialty Lens Fill Solution

CONTAMAC SOLUTIONS, INC.

Contact lens wetting solution

• Primary Device ID: 00850012123019
• NIH Device Record Key: a0586532-02f0-4704-aa43-38963f9dc59a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nutrifill
• Version Model Number: Nutrifill Samples
• Company DUNS: 117592637
• Company Name: CONTAMAC SOLUTIONS, INC.
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012123019 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181566

FDA Product Code

• MRC: Products, Contact Lens Care, Rigid Gas Permeable

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: 2022-08-12
• Device Publish Date: 2022-08-04

On-Brand Devices [Nutrifill]

• 00850012123002: Ultra-Pure Nutrient Rich Specialty Lens Fill Solution
• 00850012123019: Ultra-Pure Nutrient Rich Specialty Lens Fill Solution