PLIER 800-231

GUDID D90980023111

RAZOR TWEED ARCH BENDING PLIER

Ortho Arch Company Inc

Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers Orthodontic pliers

• Primary Device ID: D90980023111
• NIH Device Record Key: 82a21e68-d819-49b1-a7b0-520a1a86fec2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PLIER
• Version Model Number: 800-231
• Catalog Number: 800-231
• Company DUNS: 020956330
• Company Name: Ortho Arch Company 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: 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D90980023111 [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: 2023-07-06
• Device Publish Date: 2023-06-28

On-Brand Devices [PLIER]

• D90980023313: RAZOR LOOP FORMING PLIER
• D90980023111: RAZOR TWEED ARCH BENDING PLIER