2oz NEON TEAL POWDER 045-012

GUDID D7750450120

2oz NEON TEAL POWDER

GREAT LAKES ORTHODONTICS, LTD.

Dental prosthesis restorative material, unfilled resin

• Primary Device ID: D7750450120
• NIH Device Record Key: 204d1c20-dd28-4f3a-8814-c7ee406eb813
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2oz NEON TEAL POWDER
• Version Model Number: 045-012
• Catalog Number: 045-012
• Company DUNS: 041854332
• Company Name: GREAT LAKES ORTHODONTICS, LTD.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com
• Phone: 800-828-7626
• Email: info@greatlakesortho.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7750450120 [Primary]

FDA Product Code

• EBI: Resin, Denture, Relining, Repairing, Rebasing

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: 2016-09-09

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