Intraluminal Applicator Set GM11000620

GUDID 00810563022834

Intraluminal Applicator Set

Varian Medical Systems Deutschland GmbH

Bronchial brachytherapy system applicator, remote-afterloading

• Primary Device ID: 00810563022834
• NIH Device Record Key: 37082c36-cbed-45d9-9a55-30ea9c67fec7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Intraluminal Applicator Set
• Version Model Number: GM11000620
• Catalog Number: GM11000620
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• 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: true
• Expiration Date: true
• 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	00810563022834 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151022

FDA Product Code

• JAQ: System, applicator, radionuclide, remote-controlled

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: 2024-10-08
• Device Publish Date: 2024-09-30

On-Brand Devices [Intraluminal Applicator Set]

• 00816389021600: GM11000620
• 00810563022834: Intraluminal Applicator Set