TruFocus LIO Premiere 87302

GUDID 00813125015688

Laser Indirect Ophthalmoscope

IRIDEX CORPORATION

Indirect binocular laser ophthalmoscope

• Primary Device ID: 00813125015688
• NIH Device Record Key: 9fb3745c-ef9a-4836-8fd1-ccc293ffc3c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TruFocus LIO Premiere
• Version Model Number: TruFocus LIO Premiere, 810 LS
• Catalog Number: 87302
• Company DUNS: 612920785
• Company Name: IRIDEX 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: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com
• Phone: (800) 388-4747
• Email: techsupport@iridex.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813125015688 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170718

FDA Product Code

• HQF: Laser, 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: 2
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-03-28

On-Brand Devices [TruFocus LIO Premiere]

• 00813125015695: Laser Indirect Ophthalmoscope
• 00813125015688: Laser Indirect Ophthalmoscope
• 00813125015671: Laser Indirect Ophthalmoscope
• 00813125015664: Laser Indirect Ophthalmoscope
• 00813125015657: Laser Indirect Ophthalmoscope