Glass-FX Conditioner

GUDID D9560GFXCON0

D.S.I DENTAL SOLUTIONS LTD

Glass ionomer dental cement

• Primary Device ID: D9560GFXCON0
• NIH Device Record Key: 7fc8ca1b-5354-412e-8cb5-e403664d9f18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Glass-FX Conditioner
• Version Model Number: GFX-CON
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D9560GFXCON0 [Primary]

FDA Product Code

• EMA: Cement, Dental

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: 2023-02-23
• Device Publish Date: 2023-02-15

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