Disassembly pin for removal of ring cap GM11010530

GUDID 00816389025417

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

• Primary Device ID: 00816389025417
• NIH Device Record Key: 6f80d126-f21c-4340-9e4d-3a27545e936c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disassembly pin for removal of ring cap
• Version Model Number: GM11010530
• Catalog Number: GM11010530
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• 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: false
• 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	00816389025417 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150839

FDA Product Code

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

Sterilization

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

[00816389025417]

Moist Heat or Steam Sterilization

[00816389025417]

Moist Heat or Steam Sterilization

[00816389025417]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-22

On-Brand Devices [Disassembly pin for removal of ring cap]

• 00816389025417: GM11010530
• 00816389024137: GM11007390