COMPUTERIZED LENSMETER CL-300

GUDID 04562123288391

TOPCON CORPORATION

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• Primary Device ID: 04562123288391
• NIH Device Record Key: 5f2d1c4b-89b7-402c-88ae-bd5b3f8b4bbc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COMPUTERIZED LENSMETER CL-300
• Version Model Number: CL-300
• 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	04562123288391 [Primary]

FDA Product Code

• HLM: Instrument, Measuring, Lens, Ac-Powered

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: 2023-12-27
• Device Publish Date: 2023-12-19

On-Brand Devices [COMPUTERIZED LENSMETER CL-300]

• 04562123288391: CL-300
• 04562123288384: CL-300