S-Max M

GUDID 04560264560093

NAKANISHI INC.

Dental power tool system handpiece, line-powered

• Primary Device ID: 04560264560093
• NIH Device Record Key: c5868c53-56f1-45b5-8bb2-056f5b876c56
• Commercial Distribution Discontinuation: 2018-07-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: S-Max M
• Version Model Number: SG20
• 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: false
• 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	04560264560093 [Primary]

FDA Product Code

• KMW: HANDPIECE, ROTARY BONE CUTTING

Sterilization

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

[04560264560093]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-22
• Device Publish Date: 2016-09-16

On-Brand Devices [S-Max M]

• 04560264560093: SG20
• 04560264557123: SG20
• 04560264529212: SG20