Accurator Accurator A2

GUDID 00990010301221

Accurator A2, Apex Locator, compatible with G2 Endo Motor

Beyes Dental Canada Inc

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• Primary Device ID: 00990010301221
• NIH Device Record Key: 6d0d0aad-2682-43e7-bb72-e0890ca66cb9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Accurator
• Version Model Number: AL2080
• Catalog Number: Accurator A2
• Company DUNS: 244261462
• Company Name: Beyes Dental Canada Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	00990010301221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181087

FDA Product Code

• LQY: Locator, Root Apex

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: 2023-05-18
• Device Publish Date: 2023-05-10

On-Brand Devices [Accurator]

• 00837699000031: Accurator A2, Apex Locator, compatible with G2 Endo Motor
• 00837699000130: Accurator A1
• 00990010301221: Accurator A2, Apex Locator, compatible with G2 Endo Motor
• 00990010301320: Accurator A1