TRIDENT

GUDID 08053307591070

Mobile equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc

TECHNIX SPA

Mobile general-purpose fluoroscopic x-ray system, digital

• Primary Device ID: 08053307591070
• NIH Device Record Key: 2bec501b-3c1d-47ed-a603-1c3f6c9d16d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRIDENT
• Version Model Number: 2121 R 20 CS
• Company DUNS: 437977127
• Company Name: TECHNIX SPA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	08053307591070 [Primary]

FDA Product Code

• JAA: System, X-Ray, Fluoroscopic, Image-Intensified

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: 2024-11-14
• Device Publish Date: 2024-11-06

On-Brand Devices [TRIDENT]

• 08053307591087: Mobile equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc
• 08053307591070: Mobile equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc