M210 Series (Ceiling, Mobile)

GUDID 08800053064125

RATING : AC 100-240 V, 50/60 Hz, 132-178 VA

DENTIS CO. ,LTD

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• Primary Device ID: 08800053064125
• NIH Device Record Key: d49ccfe7-a096-4913-88cb-bf44d100405b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: M210 Series (Ceiling, Mobile)
• Version Model Number: M210
• 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	08800053064125 [Primary]

FDA Product Code

• FTD: Lamp, Surgical

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

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