UniLite Universal Composite 4g A1

GUDID D9560000ULA1

D.S.I DENTAL SOLUTIONS LTD

Dental composite resin

• Primary Device ID: D9560000ULA1
• NIH Device Record Key: 700464ad-509e-4132-b736-21f7ffa123e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UniLite Universal Composite 4g A1
• Version Model Number: UL-A1
• Company DUNS: 532290720
• Company Name: D.S.I DENTAL SOLUTIONS LTD
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D9560000ULA1 [Primary]

FDA Product Code

• EBF: Material, Tooth Shade, Resin

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: 2024-07-04
• Device Publish Date: 2024-06-26

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• D95600ULDAMS0 - UniLite Dam Liquid LC Material 5 syringes: 2024-07-05
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