RAZOR 800-230

GUDID D90980023010

RAZOR WEINGART PLIER

Ortho Arch Company Inc

Orthodontic pliers

• Primary Device ID: D90980023010
• NIH Device Record Key: e7b54395-6fed-4297-ab05-39241c725c58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAZOR
• Version Model Number: 800-230
• Catalog Number: 800-230
• 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	D90980023010 [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 [RAZOR]

• D90980023818: RAZOR CINCH BACK PLIER
• D90980023717: RAZOR THREE PRONG PLIER
• D90980023616: RAZOR LIGHT WIRE PLIER
• D90980023414: RAZOR OPTICAL PLIER
• D90980023212: RAZOR JARABAK PLIER
• D90980023010: RAZOR WEINGART PLIER