Ti-Max

GUDID 04560224972287

NAKANISHI INC.

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• Primary Device ID: 04560224972287
• NIH Device Record Key: 2868690d-6c93-4284-9560-ae25f705af53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ti-Max
• Version Model Number: Ti-Max TIM40J
• 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	04560224972287 [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: 2020-06-29
• Device Publish Date: 2020-06-20

On-Brand Devices [Ti-Max]

• 04560264560420: S950WL
• 04560264560413: S950SL
• 04560264560406: S950BL
• 04560264560390: S950KL
• 04560264560383: S950L
• 04560264560376: S950
• 04560224990151: S950WL
• 04560224990144: S950SL
• 04560224990137: S950BL
• 04560224989346: Ti-SG65L
• 04560224986499: Ti-SG20
• 04560224977527: S950KL
• 04560224977503: S950L
• 04560224977497: S950
• 04560224971129: Ti-SG20L
• 04560224972287: Ti-Max TIM40J