TI-MAX X CONTRA/HP

GUDID 04560264565920

NAKANISHI INC.

Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric

• Primary Device ID: 04560264565920
• NIH Device Record Key: 7613b74c-9f99-46ea-bcde-ff8faa0eccf3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TI-MAX X CONTRA/HP
• Version Model Number: X25
• 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	04560264565920 [Primary]
GS1	04560264578937 [Direct Marking]

FDA Product Code

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

Sterilization

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

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

[04560264565920]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-06
• Device Publish Date: 2020-06-26

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

• 04560264565944: X12
• 04560264565937: X15
• 04560264565920: X25
• 04560264506701: X85L
• 04560264504608: X25L
• 04560264565913: X85
• 04560264565906: X95
• 04560264565890: X12L
• 04560264565883: X15L
• 04560264565876: X20L
• 04560264565869: X25L
• 04560264565852: X85L
• 04560264565845: X95L