Titanium Lester Lens Manipulator, Angled

GUDID 00817489029466

KATALYST SURGICAL LLC

Ocular hook/spatula/manipulator, reusable

• Primary Device ID: 00817489029466
• NIH Device Record Key: 21c2569a-deb5-4eea-8d40-fbc3fb352a77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Titanium Lester Lens Manipulator, Angled
• Version Model Number: 2051A
• Company DUNS: 007883297
• Company Name: KATALYST SURGICAL LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00817489029466 [Primary]

FDA Product Code

• HNQ: Hook, Ophthalmic

Sterilization

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

[00817489029466]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-24
• Device Publish Date: 2019-06-18

On-Brand Devices [Titanium Lester Lens Manipulator, Angled ]

• 00817489029817: 2501A-6
• 00817489029466: 2051A
• 00840096202540: Titanium Lester Lens Manipulator, Angled