Philips Zoom!

GUDID 00075020035004

Discus Dental, LLC

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• Primary Device ID: 00075020035004
• NIH Device Record Key: 7b16f4a2-dfd3-4c9b-8720-7d3fdfe0d3f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Zoom!
• Version Model Number: DIS557/01
• Company DUNS: 831726109
• Company Name: Discus Dental, LLC
• Device Count: 2
• 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
GS1	00075020035004 [Primary]
GS1	00075020065780 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062176

FDA Product Code

• LBH: VARNISH, CAVITY

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-22
• Device Publish Date: 2016-09-07

On-Brand Devices [Philips Zoom!]

• 00075020035004: DIS557/01
• 00075020034991: DIS556/01
• 08710103632061: DIS5714/01