Varian Universal Interstitial Cylinder, 30mm diameter GM11013320

GUDID 00816389027886

VARIAN MEDICAL SYSTEMS, INC.

Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading

• Primary Device ID: 00816389027886
• NIH Device Record Key: 9d24a99e-8b34-4ae5-8660-bf84ceeb1a4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varian Universal Interstitial Cylinder, 30mm diameter
• Version Model Number: GM11013320
• Catalog Number: GM11013320
• Company DUNS: 009120817
• Company Name: VARIAN MEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: false
• 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	00816389027886 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193240

FDA Product Code

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

Sterilization

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

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

[00816389027886]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-03
• Device Publish Date: 2021-02-23

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