Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 2 White 209002

GUDID 07540172016513

Double-inclined plane used for separating teeth

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Dental matrix band, single-use

• Primary Device ID: 07540172016513
• NIH Device Record Key: 12991ee7-6f69-4990-bea1-f8583c91c718
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 2 White
• Version Model Number: 209002
• Catalog Number: 209002
• Company DUNS: 626406016
• Company Name: CLINICIAN'S CHOICE DENTAL PRODUCTS, 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: false
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07540172016513 [Primary]

FDA Product Code

• DZN: INSTRUMENTS, DENTAL HAND

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: 2020-03-27
• Device Publish Date: 2020-03-19