Prevest Model 3D Printing Resin 18001

GUDID D9671800100

PREVEST DENPRO LIMITED

Dental appliance fabrication material, resin

• Primary Device ID: D9671800100
• NIH Device Record Key: 90114600-3640-444f-a545-515fe0a75208
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prevest Model 3D Printing Resin
• Version Model Number: 500g plastic bottle
• Catalog Number: 18001
• Company DUNS: 859546940
• Company Name: PREVEST DENPRO LIMITED
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D9671800100 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2023-06-19
• Device Publish Date: 2023-06-09

On-Brand Devices [Prevest Model 3D Printing Resin]

• D9671800201: 1000g plastic bottle
• D9671800100: 500g plastic bottle