Elastic Separating Plier

GUDID 00190707103217

Elastic Separating Plier

ORTHO ORGANIZERS, INC.

Orthodontic pliers

• Primary Device ID: 00190707103217
• NIH Device Record Key: 8c080362-3b32-4934-8289-8bff767e8124
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elastic Separating Plier
• Version Model Number: 4150-953
• Company DUNS: 062165188
• Company Name: ORTHO ORGANIZERS, 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: 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	00190707103217 [Primary]

FDA Product Code

• JEX: PLIER, 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: 2024-01-25
• Device Publish Date: 2024-01-17

On-Brand Devices [Elastic Separating Plier]

• 00190707102340: Elastic Separating Plier
• 00190707103217: Elastic Separating Plier
• 00190707097004: Elastic Separating Plier