Central Rod Assembly

GUDID B16571130326073124034

Central rod assembly

Liberty Medical , Inc.

Vaginal brachytherapy system applicator, manual

• Primary Device ID: B16571130326073124034
• NIH Device Record Key: 0e407fb5-f675-472f-a871-818e54a57748
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Central Rod Assembly
• Version Model Number: 7113
• Company DUNS: 967592978
• Company Name: Liberty Medical , Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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
HIBCC	B16571130326073124034 [Primary]

FDA Product Code

• IWJ: System, Applicator, Radionuclide, Manual

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-24
• Device Publish Date: 2024-07-16

On-Brand Devices [Central Rod Assembly]

• B16571130325093123054: Central rod assembly
• B16571130325033023033: Central rod assembly
• B165711303261231232105: Central rod assembly
• B165711303260331240306: Central rod assembly
• B16571130326073124034: Central rod assembly