4.7 Fr. plastic-tipped catheter, 150 cm AL13115000

GUDID 00816389021280

Varian Medical Systems Deutschland GmbH

General-purpose brachytherapy system applicator, remote-afterloading

• Primary Device ID: 00816389021280
• NIH Device Record Key: ec907a39-6896-40c2-96ae-96f4157f51b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 4.7 Fr. plastic-tipped catheter, 150 cm
• Version Model Number: AL13115000
• Catalog Number: AL13115000
• Company DUNS: 332474605
• Company Name: Varian Medical Systems Deutschland GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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 Dimensions

• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter
• Length: 150 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816389021280 [Primary]
GS1	10816389021287 [Package]; Package: Pack [10 Units]; In Commercial Distribution
GS1	20816389021284 [Package]; Package: Pack [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171631

FDA Product Code

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

Sterilization

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

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

[00816389021280]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-09-19

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