Surgic Pro+

GUDID 04560264527423

NAKANISHI INC.

Dental implant system

• Primary Device ID: 04560264527423
• NIH Device Record Key: ec6d0bda-7c7a-408f-ad36-2ad1be8eefab
• Commercial Distribution Discontinuation: 2018-06-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Surgic Pro+
• Version Model Number: Surgic Pro+ OPT(230V)
• 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	04560264527423 [Primary]

FDA Product Code

• EBW: CONTROLLER, FOOT, HANDPIECE AND CORD

Sterilization

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

[04560264527423]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-29
• Device Publish Date: 2016-09-16

On-Brand Devices [Surgic Pro+]

• 04560264560062: Surgic Pro+ OPT-D(120V)
• 04560264560031: Surgic Pro+ OPT(120V)
• 04560264530263: Surgic Pro+ OPT-D(120V)
• 04560264530256: Surgic Pro+ OPT(120V)
• 04560264528598: Surgic Pro+ OPT-D(230V)
• 04560264527423: Surgic Pro+ OPT(230V)