Gynecological Brachytherapy Kit

GUDID B16570580325033023065

Gynecological brachytherapy kit

Liberty Medical , Inc.

Vaginal brachytherapy system applicator, manual

• Primary Device ID: B16570580325033023065
• NIH Device Record Key: 817d20a8-07c6-4175-8b13-68c579c76348
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gynecological Brachytherapy Kit
• Version Model Number: 7058
• 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	B16570580325033023065 [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: 2023-11-03
• Device Publish Date: 2023-10-26

On-Brand Devices [Gynecological Brachytherapy Kit]

• B16570580325093023155: Gynecological brachytherapy kit
• B16570580325033023065: Gynecological brachytherapy kit
• B16570580325113023196: Gynecological brachytherapy kit
• B16570580325113024015: Gynecological brachytherapy kit
• B16570580326033124040: Gynecological brachytherapy kit
• B16570580326073124097: Gynecological brachytherapy kit