RTgo

GUDID 00884838092112

MR-RT RTgo software USB stick

Philips Oy

MRI system application software

• Primary Device ID: 00884838092112
• NIH Device Record Key: c3906e5c-1c31-4624-bcdf-b066529d3a05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RTgo
• Version Model Number: 459801266633
• Company DUNS: 539852079
• Company Name: Philips Oy
• Device Count: 1
• DM Exempt: true
• 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: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: +1(800)722-9377
• Email: healthcare@philips.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838092112 [Primary]

FDA Product Code

• MUJ: System, planning, radiation therapy treatment

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: 2019-06-17
• Device Publish Date: 2019-06-07

On-Brand Devices [RTgo]

• 00884838084667: MR-RT RTgo software USB stick
• 00884838092112: MR-RT RTgo software USB stick