Grub screws for clamping unit (pack of 10) GM11009950

GUDID 00810563022193

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: 00810563022193
• NIH Device Record Key: d728e873-d67d-4dc6-b822-b3c3fa8fa1ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Grub screws for clamping unit (pack of 10)
• Version Model Number: GM11009950
• Catalog Number: GM11009950
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• Device Count: 10
• 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	00810563022193 [Unit of Use]
GS1	10810563022190 [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

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

Moist Heat or Steam Sterilization

[00810563022193]

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

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