M65

GUDID 04560264565036

NAKANISHI INC.

Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric

• Primary Device ID: 04560264565036
• NIH Device Record Key: 31cea308-d6dd-494d-bf54-3d6cf7dbd495
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: M65
• Version Model Number: M65
• Company DUNS: 690710546
• Company Name: NAKANISHI 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: 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	04560264565036 [Direct Marking]
GS1	04560264578234 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230106

FDA Product Code

• EGS: Handpiece, contra- and right-angle attachment, dental

Sterilization

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

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

[04560264565036]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-16
• Device Publish Date: 2023-10-06

On-Brand Devices [M65]

• 04560264572881: M65
• 04560264565036: M65