Spacer 5.5mm Synthetic 150 piece SS9X55150

GUDID 00815165020240

Eckert & Ziegler Bebig, Inc.

Manual brachytherapy system

• Primary Device ID: 00815165020240
• NIH Device Record Key: e49d90c7-15c1-484d-abd9-a6c1b6e59fe8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spacer 5.5mm Synthetic 150 piece
• Version Model Number: Spacer 5.5mm Synthetic 150 piece
• Catalog Number: SS9X55150
• Company DUNS: 021125001
• Company Name: Eckert & Ziegler Bebig, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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	00815165020240 [Primary]

FDA Product Code

• KXK: Source, Brachytherapy, Radionuclide

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-15
• Device Publish Date: 2015-10-27

On-Brand Devices [Spacer 5.5mm Synthetic 150 piece]

• 00081516502024: Spacer 5.5mm Synthetic 150 piece
• 00815165020240: Spacer 5.5mm Synthetic 150 piece