BONE TIP/BM-EX01R

GUDID 04719873120833

BONART CO., LTD.

Dental ultrasonic surgical system

• Primary Device ID: 04719873120833
• NIH Device Record Key: e4fda4fd-57b1-453e-aa35-3b79cf625e52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BONE TIP/BM-EX01R
• Version Model Number: BM-EX01R
• Company DUNS: 657263687
• Company Name: BONART CO., LTD.
• 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: 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	04719873120833 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080761

FDA Product Code

• DZI: Drill, Bone, Powered

Sterilization

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

[04719873120833]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-31
• Device Publish Date: 2017-01-19

Devices Manufactured by BONART CO., LTD.

• 04719873121533 - ART TRIPLE BEND 25kHz: 2023-04-03
• 04719873121540 - ART TRIPLE BEND 30kHz: 2023-04-03
• 04719873121410 - PIEZO TIP/BE-P: 2022-03-28
• 04719873121366 - 25K FS-SLIM PLASTIC INSERT/Darby: 2021-01-04
• 04719873121373 - 30K FS-SLIM PLASTIC INSERT/Darby: 2021-01-04
• 04719873121380 - 25K FS-10 PLASTIC INSERT/Darby: 2021-01-04
• 04719873121397 - 30K FS-10 PLASTIC INSERT/Darby: 2021-01-04
• 04719873121359 - BONE TIP/BM-PS1: 2020-09-25