KATENA K30-1650

GUDID 10841668144470

Wide-Angle Viewing RS Lens

KATENA PRODUCTS, INC.

Vitrectomy contact lens, single-use

• Primary Device ID: 10841668144470
• NIH Device Record Key: d8fdcd34-b552-454b-a856-8424966f6a85
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KATENA
• Version Model Number: K30-1650
• Catalog Number: K30-1650
• Company DUNS: 085668598
• Company Name: KATENA PRODUCTS, INC.
• 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: 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	00841668144473 [Primary]
GS1	10841668144470 [Package]; Contains: 00841668144473; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• HJK: Lens, contact, polymethylmethacrylate, diagnostic

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: 2026-03-10
• Device Publish Date: 2026-03-02

On-Brand Devices [KATENA]

• 10841668146474: Tonometer Prism
• 10841668144470: Wide-Angle Viewing RS Lens
• 10841668144463: High-Mag RS Lens
• 10841668123949: Flat Vitrectomy Lens w fixed ring
• 10841668123338: ROP Kit