ST500 Series

GUDID 08800053091237

AC 100-240V, 50/60Hz, 500VA

DENTIS CO. ,LTD

Electromechanical operating table base

• Primary Device ID: 08800053091237
• NIH Device Record Key: f531b037-56e8-4a96-8e0d-1a9b91e9a8c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ST500 Series
• Version Model Number: ST500
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800053091237 [Primary]

FDA Product Code

• GDC: Table, Operating-Room, Electrical

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: 2025-05-02
• Device Publish Date: 2025-04-24

On-Brand Devices [ST500 Series]

• 08800053091244: AC 100-240V, 50/60Hz, 500VA
• 08800053091237: AC 100-240V, 50/60Hz, 500VA