Maxso M200

GUDID 00628504370063

M200-M/M4, M4 Backend, Triple Spray, Non-Optic

Beyes Dental Canada Inc

Dental power tool system handpiece, pneumatic

• Primary Device ID: 00628504370063
• NIH Device Record Key: 7de061e1-e609-4e50-9c93-2b4e691fd61a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maxso M200
• Version Model Number: HP2009
• Company DUNS: 244261462
• Company Name: Beyes Dental Canada 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	00628504370063 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101551

FDA Product Code

• EFB: Handpiece, Air-Powered, Dental

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-22
• Device Publish Date: 2019-04-12

On-Brand Devices [Maxso M200]

• 00628504370087: M200-M/QD, Beyes QD Backend, Triple Spray, Non-Optic
• 00628504370063: M200-M/M4, M4 Backend, Triple Spray, Non-Optic