KEATS TWEEZERS

GUDID 00190707065850

KEATS BRACKET PLACING REVERSE ACTION TWEEZER

ORTHO ORGANIZERS, INC.

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• Primary Device ID: 00190707065850
• NIH Device Record Key: ae79df6f-62a1-493a-b5fc-24b53ce1a23b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KEATS TWEEZERS
• Version Model Number: 4260-344
• Company DUNS: 062165188
• Company Name: ORTHO ORGANIZERS, 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: 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	00190707065850 [Primary]

FDA Product Code

• ECQ: ALIGNER, BRACKET, 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: 2020-07-21
• Device Publish Date: 2020-07-13

On-Brand Devices [KEATS TWEEZERS]

• 00190707065850: KEATS BRACKET PLACING REVERSE ACTION TWEEZER
• 00190707065843: KEATS BRACKET PLACING TWEEZER