TI-MAX nano CONTRA/HP

GUDID 04560264566019

NAKANISHI INC.

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• Primary Device ID: 04560264566019
• NIH Device Record Key: 9fc1e5f1-05bc-462c-87b4-52420852f4c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TI-MAX nano CONTRA/HP
• Version Model Number: nano25LS
• 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	04560264535145 [Direct Marking]
GS1	04560264566019 [Primary]

FDA Product Code

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

Sterilization

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

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

[04560264566019]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-11-28
• Device Publish Date: 2020-06-12

On-Brand Devices [TI-MAX nano CONTRA/HP]

• 04560264566019: nano25LS
• 04560264566002: nano95LS