Triton Needles

GUDID 00812444026764

BRACHYTHERAPY

RIVERPOINT MEDICAL, LLC

Brachytherapy needle

• Primary Device ID: 00812444026764
• NIH Device Record Key: def99cbe-edd8-4d71-8a76-822abf4b0dc0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Triton Needles
• Version Model Number: TN 1031-1820
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812444026764 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103449

FDA Product Code

• KXK: Source, Brachytherapy, Radionuclide

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-07-27

On-Brand Devices [Triton Needles]

• 00812444027877: Brachytherapy
• 00812444026764: BRACHYTHERAPY