Direct Bond Eyelets

GUDID 00190730088277

Rectangle Direct Bond Eyelet 10 per pack

ORTHO TECHNOLOGY, INC.

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• Primary Device ID: 00190730088277
• NIH Device Record Key: 8f8a3c7a-8bc2-403a-88ce-76e2713e28de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Direct Bond Eyelets
• Version Model Number: 025-000
• Company DUNS: 781772017
• Company Name: ORTHO TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190730088277 [Primary]

FDA Product Code

• EJF: BRACKET, METAL, 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: 2021-09-24
• Device Publish Date: 2021-09-16

On-Brand Devices [Direct Bond Eyelets]

• 00190730011718: Round Direct Bond Eyelet 10 per pack
• 00190730088277: Rectangle Direct Bond Eyelet 10 per pack