myQuickmat Prime Kit 6890

GUDID E29968900

Polydentia SA

Dental matrix band kit

• Primary Device ID: E29968900
• NIH Device Record Key: 80870eb6-a720-47ec-ab33-13e34e4553c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myQuickmat Prime Kit
• Version Model Number: 6890
• Catalog Number: 6890
• Company DUNS: 481461598
• Company Name: Polydentia SA
• 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: 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	E29968900 [Primary]

FDA Product Code

• DZN: Instruments, Dental Hand

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

[E29968900]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-24
• Device Publish Date: 2025-06-16

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