Landers 50° Prism Lens

GUDID 00630238008655

OCULAR INSTRUMENTS, INC.

Vitrectomy contact lens, reusable

• Primary Device ID: 00630238008655
• NIH Device Record Key: 4084f2b5-55a8-4ecb-b745-7a9c0716a947
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Landers 50° Prism Lens
• Version Model Number: OLV-8
• Company DUNS: 046212387
• Company Name: OCULAR INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	00630238008655 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K941420

FDA Product Code

• HJK: Lens, Contact, Polymethylmethacrylate, Diagnostic

Sterilization

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

[00630238008655]

Moist Heat or Steam Sterilization

[00630238008655]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-17
• Device Publish Date: 2016-12-12

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