L200 Series (Ceiling, Mobile)

GUDID 08806169141309

AC 100 - 240 V, 67 VA, 50/60 Hz

DENTIS CO. ,LTD

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• Primary Device ID: 08806169141309
• NIH Device Record Key: ab17a1bf-fe86-464d-aab3-4c3a58efc6b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: L200 Series (Ceiling, Mobile)
• Version Model Number: L200
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806169141309 [Primary]

FDA Product Code

• FTD: Lamp, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-07-27
• Device Publish Date: 2016-12-27

On-Brand Devices [L200 Series (Ceiling, Mobile)]

• 08806169141309: AC 100 - 240 V, 67 VA, 50/60 Hz
• 08800053063005: RATING : AC 100-240 V, 50/60 Hz, 163 VA