S250 Series(Ceiling, Mobile)

GUDID 08800053093712

AC 100-240V, 50/60HZ, 61-94VA

DENTIS CO. ,LTD

Operating room light system

• Primary Device ID: 08800053093712
• NIH Device Record Key: 0df0229e-875d-4ace-9c72-19a84e0ee898
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: S250 Series(Ceiling, Mobile)
• Version Model Number: S250-23001
• 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	08800053093712 [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: 2024-11-06
• Device Publish Date: 2024-10-29

On-Brand Devices [S250 Series(Ceiling, Mobile)]

• 08800053093750: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093736: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093729: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093712: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093705: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093682: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093675: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093668: AC 100-240V, 50/60Hz, 61-94VA
• 08800053093651: AC 100-240V, 50/60HZ, 61-94VA
• 08800053093743: AC 100-240V, 50/60HZ, 61-94VA