Flexible Catheter Single Leader, D=1.65mm, L=300mm LLA300-F

GUDID 04049223118259

Eckert & Ziegler BEBIG GmbH

General-purpose brachytherapy system applicator, remote-afterloading

• Primary Device ID: 04049223118259
• NIH Device Record Key: ca6f1fb7-23c7-4229-8a20-6fa556b05a9c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flexible Catheter Single Leader, D=1.65mm, L=300mm
• Version Model Number: LLA300-F#02-5PC
• Catalog Number: LLA300-F
• Company DUNS: 331080432
• Company Name: Eckert & Ziegler BEBIG GmbH
• Device Count: 5
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com
• Phone: +4930941084130
• Email: info@bebig.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049223118259 [Primary]
GS1	04049223119089 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142986

FDA Product Code

• JAQ: System, Applicator, Radionuclide, Remote-Controlled

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-10-06

On-Brand Devices [Flexible Catheter Single Leader, D=1.65mm, L=300mm]

• 04049223118259: LLA300-F#02-5PC
• 04049223101077: LLA300-F#02-SP