RTS Brachytherapy Kit I-125 RTSKITI125

GUDID 00081516502017

Eckert & Ziegler Bebig, Inc.

Manual brachytherapy system

• Primary Device ID: 00081516502017
• NIH Device Record Key: 32e31c9d-01b6-47df-9317-2bf506a2416f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RTS Brachytherapy Kit I-125
• Version Model Number: RTS Brachytherapy Kit I-125
• Catalog Number: RTSKITI125
• Company DUNS: 021125001
• Company Name: Eckert & Ziegler Bebig, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does n
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 203-262-0571
• Email: ned.lanfranco@bebig.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00081516502017 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-27

On-Brand Devices [RTS Brachytherapy Kit I-125]

• 00081516502017: RTS Brachytherapy Kit I-125
• 00815165020172: RTS Brachytherapy Kit I-125