Vivid QwikTemp C&B

GUDID D724N1104540

A2

PEARSON DENTAL SUPPLIES, INC.

Temporary dental crown/bridge resin

• Primary Device ID: D724N1104540
• NIH Device Record Key: e568059a-c663-4bbc-bc6b-70f0a7a8b839
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vivid QwikTemp C&B
• Version Model Number: N110454
• Company DUNS: 082874108
• Company Name: PEARSON DENTAL SUPPLIES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D724N1104540 [Primary]

FDA Product Code

• EBG: Crown And Bridge, Temporary, Resin

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-10-29
• Device Publish Date: 2016-06-23

On-Brand Devices [Vivid QwikTemp C&B]

• D724N1104590: C2
• D724N1104580: B1
• D724N1104560: A3
• D724N1104540: A2
• D724N1104520: A1
• D724N1104500: Bleach