RTS Brachytherapy Kit PD103 RTSKITPD103

GUDID 00081516502018

Eckert & Ziegler Bebig, Inc.

Manual brachytherapy system

• Primary Device ID: 00081516502018
• NIH Device Record Key: 11223c44-d8f4-4e67-952e-b22b2aca388e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RTS Brachytherapy Kit PD103
• Version Model Number: RTS Brachytherapy Kit PD103
• Catalog Number: RTSKITPD103
• 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: false
• 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	00081516502018 [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 PD103]

• 00081516502018: RTS Brachytherapy Kit PD103
• 00815165020189: RTS Brachytherapy Kit PD103