Universal Endometrial Applicator Set GM11009840

GUDID 00810563022100

Varian Medical Systems Deutschland GmbH

Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading

• Primary Device ID: 00810563022100
• NIH Device Record Key: c15a1531-ce89-4a03-81ec-550af4b9e858
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Universal Endometrial Applicator Set
• Version Model Number: GM11009840
• Catalog Number: GM11009840
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00810563022100 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K980576

FDA Product Code

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

Sterilization

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

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

[00810563022100]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-24
• Device Publish Date: 2023-04-16

On-Brand Devices [Universal Endometrial Applicator Set]

• 00816389025035: GM11009840
• 00810563022100: GM11009840