Visionix VSN5200FB

GUDID 04580606431751

Fireworks Chart SET

RIGHT MFG. CO., LTD.

Automated ophthalmic refractometer

• Primary Device ID: 04580606431751
• NIH Device Record Key: aeb8a389-d0c0-4614-97f5-96a58e046935
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Visionix
• Version Model Number: Retinomax K-plus5
• Catalog Number: VSN5200FB
• Company DUNS: 713383495
• Company Name: RIGHT MFG. CO., LTD.
• 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	04580606431751 [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: 2023-01-13
• Device Publish Date: 2023-01-05

On-Brand Devices [Visionix]

• 04580606431850: Bear Chart SET
• 04580606431843: Fireworks Chart SET
• 04580606431836: Tulip Chart SET
• 04580606431768: Bear Chart SET
• 04580606431751: Fireworks Chart SET
• 04580606431744: Tulip Chart SET
• 04580606431652: Tulip Chart SET
• 04580606431584: DIGITAL PHOTO UNIT SET
• 04580606431553: DIGITAL PHOTO UNIT SET
• 04580606431522: CLINICAL UNIT SET
• 04580606431492: CLINICAL UNIT SET