Length cutting gauge, 250mm for implant tubes and breast applicators up to 6 Fr. GM11010030

GUDID 00816389029095

Varian Medical Systems Deutschland GmbH

General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading General-purpose brachytherapy system applicator, remote-afterloading

• Primary Device ID: 00816389029095
• NIH Device Record Key: b9390183-2e9f-403c-bbd2-d585d75a5c14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Length cutting gauge, 250mm for implant tubes and breast applicators up to 6 Fr.
• Version Model Number: GM11010030
• Catalog Number: GM11010030
• 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	00816389029095 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983436

FDA Product Code

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

Sterilization

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

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

[00816389029095]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-25
• Device Publish Date: 2021-11-17

On-Brand Devices [Length cutting gauge, 250mm for implant tubes and breast applicators up to 6 Fr.]

• 00816389025172: GM11010030
• 00816389029095: GM11010030