Philips Zoom

GUDID 08710103611967

Discus Dental, LLC

Radiation shielding goggles/spectacles

• Primary Device ID: 08710103611967
• NIH Device Record Key: a81e47a0-60f2-4121-8fa4-6dae81113144
• Commercial Distribution Discontinuation: 2024-01-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Zoom
• Version Model Number: DIS203/30
• Company DUNS: 831726109
• Company Name: Discus Dental, LLC
• Device Count: 1
• DM Exempt: false
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08710103611967 [Primary]

FDA Product Code

• IWS: Shield, eye, radiological

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: 2024-01-30
• Device Publish Date: 2020-09-20

On-Brand Devices [Philips Zoom]

• 08710103632092: DIS574/01
• 08710103632085: DIS573/01
• 00075020044129: DIS716/01
• 08710103632122: DIS578/01
• 00075020035011: DIS558/01
• 08710103611967: DIS203/30