Lumindex 3 LED Transilluminator Standard 3mm Light Guide 71-18836

GUDID 00723896009079

PRACTICON, INC.

ENT transilluminator

• Primary Device ID: 00723896009079
• NIH Device Record Key: 85da3f9c-e8fe-4682-8a76-44ef02713d56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumindex 3 LED Transilluminator Standard 3mm Light Guide
• Version Model Number: 7118836
• Catalog Number: 71-18836
• Company DUNS: 119193803
• Company Name: PRACTICON, INC.
• 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: false
• 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	00723896009079 [Primary]

FDA Product Code

• HJN: Transilluminator, Battery-Powered

Sterilization

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

[00723896009079]

Moist Heat or Steam Sterilization

[00723896009079]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-20
• Device Publish Date: 2018-07-20

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