NLZ

GUDID 04560264551275

NAKANISHI INC.

Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Dental power tool system, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered

• Primary Device ID: 04560264551275
• NIH Device Record Key: 055eb67d-8a7d-489d-a552-3820b2f42707
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NLZ
• Version Model Number: NLZ E U
• 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	04560264551275 [Primary]

FDA Product Code

• EBW: Controller, foot, handpiece and cord

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: 2020-07-15
• Device Publish Date: 2020-07-07

On-Brand Devices [NLZ]

• 04560264551305: NLZ Endo
• 04560264566453: NLZ CDE
• 04560264551374: NLZ
• 04560264551282: NLZ U
• 04560264551275: NLZ E U
• 04560264551268: NLZ CD
• 04560264551251: NLZ CDL
• 04560264551213: NLZ S120
• 04560264551206: NLZ E S120