Oculus Disposable Vitrectomy Lens Flat,10 Pack

GUDID 00630238117500

OCULAR INSTRUMENTS, INC.

Vitrectomy contact lens, single-use

• Primary Device ID: 00630238117500
• NIH Device Record Key: edc8b60f-d1d6-4367-b776-3775b85614aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Oculus Disposable Vitrectomy Lens Flat,10 Pack
• Version Model Number: 55110 12184
• Company DUNS: 046212387
• Company Name: OCULAR INSTRUMENTS, INC.
• Device Count: 10
• 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	00063023812184 [Unit of Use]
GS1	00630238117500 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012096

FDA Product Code

• HJK: Lens, Contact, Polymethylmethacrylate, Diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-09

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