Endoillumination Probe, including illuminated scleral depressor.(23 gauge / 0.6

GUDID 18717872035489

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Ophthalmic fibreoptic light instrument, single-use

• Primary Device ID: 18717872035489
• NIH Device Record Key: f0ce7b5d-e263-4012-aa0d-e327e0dc725f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endoillumination Probe, including illuminated scleral depressor.(23 gauge / 0.6
• Version Model Number: 3269.D06-00
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• Device Count: 6
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	08717872035482 [Primary]
GS1	18717872035489 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062895

FDA Product Code

• MPA: Endoilluminator

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-08
• Device Publish Date: 2025-03-31

On-Brand Devices [Endoillumination Probe, including illuminated scleral depressor.(23 gauge / 0.6 ]

• 08717872009414: 3269.D06
• 18717872035489: 3269.D06-00