RetinaStation 700-C1101-231

GUDID 04719876420060

Non-Mydriatic Auto Fundus Camera

CRYSTALVUE MEDICAL CORPORATION

Ophthalmic fundus camera

• Primary Device ID: 04719876420060
• NIH Device Record Key: 2db534ec-f199-4c27-8655-36c00c107a7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RetinaStation
• Version Model Number: RetinaStation
• Catalog Number: 700-C1101-231
• Company DUNS: 658841648
• Company Name: CRYSTALVUE MEDICAL CORPORATION
• 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: 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

Customer Support Contacts

• Phone: +88633607711
• Email: Oliver.Lin@crystalvue.com.tw

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719876420060 [Primary]

FDA Product Code

• HKI: Camera, Ophthalmic, 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: 2020-07-02
• Device Publish Date: 2020-02-04

Devices Manufactured by CRYSTALVUE MEDICAL CORPORATION

• 04719876420398 - Vitazi View™: 2024-05-28 Automated Portable Retinal Camera
• 04719876420268 - NFC-600: 2021-07-19 Automated Portable Retinal Camera
• 04719876420275 - Halo: 2021-07-19 Automated Portable Retinal Camera
• 04719876420176 - Polaris: 2020-07-28 Non-Mydriatic Auto Fundus Camera
• 04719876420060 - RetinaStation: 2020-07-02Non-Mydriatic Auto Fundus Camera
• 04719876420060 - RetinaStation: 2020-07-02 Non-Mydriatic Auto Fundus Camera
• 04719876420053 - NFC-700: 2020-07-02 Non-Mydriatic Auto Fundus Camera