RETINAL CAMERA TRC-50DX

GUDID 04571130282643

TOPCON CORPORATION

Ophthalmic fundus camera

• Primary Device ID: 04571130282643
• NIH Device Record Key: 6cc523ed-1fad-4788-ab17-cfa9c5f0e1fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RETINAL CAMERA TRC-50DX
• Version Model Number: TRC-50DX
• Company DUNS: 690542881
• Company Name: TOPCON 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04571130282643 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-30
• Device Publish Date: 2021-08-20

On-Brand Devices [RETINAL CAMERA TRC-50DX]

• 04562123288278: TRC-50DX
• 04571130282643: TRC-50DX
• 04571130282636: TRC-50DX