ContactPro

GUDID 20789594000903

YOUNG MICROBRUSH, LLC

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• Primary Device ID: 20789594000903
• NIH Device Record Key: c5358aae-db64-427f-aa36-d62f4fbe8fac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ContactPro
• Version Model Number: 291750
• Company DUNS: 929236305
• Company Name: YOUNG MICROBRUSH, LLC
• 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: 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
GS1	00789594000909 [Primary]
GS1	10789594000906 [Package]; Contains: 00789594000909; Package: [300 Units]; In Commercial Distribution
GS1	20789594000903 [Package]; Contains: 10789594000906; Package: [12 Units]; In Commercial Distribution

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: 2020-12-16
• Device Publish Date: 2020-12-08

On-Brand Devices [ContactPro]

• 20789594000903: 291750
• 10789594000890: 291749
• 10789594000883: 291748
• 10789594000876: 291747
• 10789594000869: 291746
• 10789594000821: 291709
• 10789594000814: 291708
• 10789594000807: 291707
• 10789594000791: 291706
• 20789594000781: 291705
• 20789594000774: 291704