NLX

GUDID 04560264523104

NAKANISHI INC.

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 Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric Dental surgical power tool motor, electric

• Primary Device ID: 04560264523104
• NIH Device Record Key: 323a9a42-3bea-4856-8362-6628292b77c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NLX
• Version Model Number: NLX plus
• 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	04560264523104 [Primary]
GS1	04589551382965 [Direct Marking]

FDA Product Code

• EBW: Controller, foot, handpiece and cord

Sterilization

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

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

[04560264523104]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-11-25
• Device Publish Date: 2020-11-13

On-Brand Devices [NLX]

• 04560264522237: NLX nano U
• 04560264521193: NLX nano
• 04560264573628: NLX nano U
• 04560264573307: NLX nano S120
• 04560264572836: NLX CDE
• 04560264572829: NLX CD
• 04560264572812: NLX nano
• 04560264534568: NLX nano S120E
• 04560264523104: NLX plus