QuickmatFIT 5805

GUDID E29958059

anatomical sectional matrices 0.04mm premolar

Polydentia SA

Dental matrix band, single-use

• Primary Device ID: E29958059
• NIH Device Record Key: 06386475-108c-4315-9348-00a4deabdb01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QuickmatFIT
• Version Model Number: 5805
• Catalog Number: 5805
• Company DUNS: 481461598
• Company Name: Polydentia SA
• Device Count: 50
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E29958050 [Primary]
HIBCC	E29958059 [Unit of Use]

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: 2024-02-06
• Device Publish Date: 2024-01-29

On-Brand Devices [QuickmatFIT ]

• E29958569: anatomical sectional matrices 0.04mm molar deep
• E29958469: anatomical sectional matrices 0.04mm molar deep
• E29958369: anatomical sectional matrices 0.04mm molar
• E29958359: anatomical sectional matrices 0.04mm premolar
• E29958069: anatomical sectional matrices 0.04mm molar
• E29958059: anatomical sectional matrices 0.04mm premolar