iProphy mobile

GUDID 04560264539211

NAKANISHI INC.

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• Primary Device ID: 04560264539211
• NIH Device Record Key: b3a02c6a-97a3-45e1-9d9a-aaf7afa1b782
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iProphy mobile
• Version Model Number: iProphy mobile Stand
• 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	04560264539211 [Primary]

FDA Product Code

• EKX: Handpiece, direct drive, ac-powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-10-12
• Device Publish Date: 2020-06-18

On-Brand Devices [iProphy mobile]

• 04560264539211: iProphy mobile Stand
• 04560264564213: iProphy mobile Motor
• 04560264559707: iProphy mobile Complete Set