Ulysses Extrusion Spring 855-211

GUDID 00190746146138

FIXED FUNCT ULYSSES/EXTRUSION SPRING 10/PKG

AMERICAN ORTHODONTICS CORPORATION

Orthodontic spring Orthodontic spring

• Primary Device ID: 00190746146138
• NIH Device Record Key: 771938b6-3502-4253-bcfe-53185ebb1927
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ulysses Extrusion Spring
• Version Model Number: 855-211
• Catalog Number: 855-211
• Company DUNS: 044668515
• Company Name: AMERICAN ORTHODONTICS CORPORATION
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-558-7687
• Email: info@americanortho.com
• Phone: 800-558-7687
• Email: info@americanortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190746146138 [Primary]

FDA Product Code

• ECO: Spring, Orthodontic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-24
• Device Publish Date: 2019-04-16

On-Brand Devices [Ulysses Extrusion Spring]

• 00190746146138: FIXED FUNCT ULYSSES/EXTRUSION SPRING 10/PKG
• 00190746074325: FIXED FUNCT ULYSSES/EXTRUSION SPRING 10/PKG