REFRACTION SYSTEM Chronos

GUDID 04571130282773

TOPCON CORPORATION

Automated ophthalmic refractometer

• Primary Device ID: 04571130282773
• NIH Device Record Key: 76cb3d2f-1741-4914-9cd0-0e29a5285879
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REFRACTION SYSTEM Chronos
• Version Model Number: Chronos
• Company DUNS: 690542881
• Company Name: TOPCON 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04571130282773 [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: 2024-08-09
• Device Publish Date: 2024-08-01

On-Brand Devices [REFRACTION SYSTEM Chronos]

• 04571130282520: Chronos
• 04571130282773: Chronos