Benda Brush

GUDID 00817051022611

Benda Brush Mini Blue

CENTRIX, INC.

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• Primary Device ID: 00817051022611
• NIH Device Record Key: e146590e-cf98-45fd-9f22-542ddd027db0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Benda Brush
• Version Model Number: 370602
• Company DUNS: 053707303
• Company Name: CENTRIX, INC.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817051022611 [Primary]

FDA Product Code

• KXR: Applicator, Resin

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: 2024-01-08
• Device Publish Date: 2023-12-29

On-Brand Devices [Benda Brush]

• 00817051023496: Benda Brush Mini Red
• 00817051023489: Benda Brush Regular Blue
• 00817051023472: Benda Brush Regular Multi-colors
• 00817051022635: Benda Brush Mini Green
• 00817051022628: Benda Brush Mini Yellow
• 00817051022611: Benda Brush Mini Blue
• 00817051022604: Benda Brush Mini Red
• 00817051022598: Benda Brush Regular Green
• 00817051022581: Benda Brush Regular Yellow
• 00817051022574: Benda Brush Regular BLUE
• 00817051022567: Benda Brush Regular Red