AUTO REFKERATOMETER

GUDID 04582273612273

100V

TOMEY CORPORATION.

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• Primary Device ID: 04582273612273
• NIH Device Record Key: 931acdb5-b04c-421d-8762-8c1e9a12eda5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AUTO REFKERATOMETER
• Version Model Number: RC-800
• Company DUNS: 696280002
• Company Name: TOMEY CORPORATION.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04582273612273 [Primary]

FDA Product Code

• HKO: Refractometer, Ophthalmic

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: 2020-11-09
• Device Publish Date: 2020-10-30

On-Brand Devices [AUTO REFKERATOMETER]

• 04582273612273: 100V
• 04582273612242: 100V
• 04582273611788: RC-800
• 04582273600218: RC-5000