LUVIS-C600 Series

GUDID 08800053045032

AC 100-240 V, 50-60 Hz, 30-45 VA

DENTIS CO. ,LTD

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• Primary Device ID: 08800053045032
• NIH Device Record Key: f68d6cad-a76a-4f30-a287-1b192ae38427
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUVIS-C600 Series
• Version Model Number: C600-H0S0A1
• Company DUNS: 694721181
• Company Name: DENTIS CO. ,LTD
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• 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	08800053045032 [Primary]

FDA Product Code

• EAZ: Light, Operating, 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: 2024-01-31
• Device Publish Date: 2024-01-23

On-Brand Devices [LUVIS-C600 Series]

• 08800053053815: AC 12-24 V, 50/60 Hz, 20-21 VA
• 08800053053808: AC 12-24 V, 50/60 Hz, 20-21 VA
• 08800053053792: AC 12-24 V, 50/60 Hz, 20-21 VA
• 08800053053785: AC 12-24 V, 50/60 Hz, 20-21 VA
• 08800053045063: AC 100-240 V, 50-60 Hz, 30-45 VA
• 08800053045056: AC 100-240 V, 50-60 Hz, 30-45 VA
• 08800053045049: AC 100-240 V, 50-60 Hz, 30-45 VA
• 08800053045032: AC 100-240 V, 50-60 Hz, 30-45 VA