Elastic Directors

GUDID 00190730007292

Elastic Directors Multicolored 100 per pack

ORTHO TECHNOLOGY, INC.

Orthodontic inter-arch elastic band

• Primary Device ID: 00190730007292
• NIH Device Record Key: 05c6f20d-8cd0-4904-86c7-196b7dcc4a7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elastic Directors
• Version Model Number: 500-307
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190730007292 [Primary]

FDA Product Code

• ECI: BAND, ELASTIC, ORTHODONTIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-27

Devices Manufactured by ORTHO TECHNOLOGY, INC.

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• 00190730084835 - Ortho Technology: 2024-09-26 DLR-Bracket Height Gage Alum018
• 00190730084842 - Ortho Technology: 2024-09-26 Bracket Height Gauge Alum 022
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