Medium Prostate Template

GUDID B16556510326063024036

medium prostate template

Liberty Medical , Inc.

Prostate brachytherapy system applicator, manual

• Primary Device ID: B16556510326063024036
• NIH Device Record Key: 0fa0f3c1-10a7-41dd-9aee-6a1bd510b1b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medium Prostate Template
• Version Model Number: 5651
• 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	B16556510326063024036 [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 [Medium Prostate Template]

• B16556510325113023172: medium prostate template
• B16556510326033123199: medium prostate template
• B16556510326063024036: medium prostate template