Iplan Rt Dose, Iplan Rt Adaptive, Iplan Rt Phantom 21381E

GUDID 04056481000592

Brainlab AG

Radiation therapy software

• Primary Device ID: 04056481000592
• NIH Device Record Key: 8a6e665e-d6ed-48a7-8ed7-1c61eeb685b1
• Commercial Distribution Discontinuation: 2017-06-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Iplan Rt Dose, Iplan Rt Adaptive, Iplan Rt Phantom
• Version Model Number: 4.5
• Catalog Number: 21381E
• Company DUNS: 314482980
• Company Name: Brainlab AG
• 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: true
• 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: +49899915680
• Email: contact@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481000592 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080888

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-15

On-Brand Devices [Iplan Rt Dose, Iplan Rt Adaptive, Iplan Rt Phantom]

• 04056481138608: 4.5
• 04056481000592: 4.5