Kelowna GYN Template for 17 gauge (1.47 mm) needles GM11012220

GUDID 00816389020238

Including locking collets (pack of 25) and needle collet wrench

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

• Primary Device ID: 00816389020238
• NIH Device Record Key: 0aecedb1-00db-4823-b473-c9cf8f06b172
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kelowna GYN Template for 17 gauge (1.47 mm) needles
• Version Model Number: GM11012220
• Catalog Number: GM11012220
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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	00816389020238 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232949

FDA Product Code

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

Sterilization

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

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

[00816389020238]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-27
• Device Publish Date: 2024-02-19

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