LTEX

GUDID 05060792970962

Litex Manufacturing, Inc.

Medical equipment handle cover adaptor

• Primary Device ID: 05060792970962
• NIH Device Record Key: d77b8638-2567-44f0-b0a6-6ff45c8ac889
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LTEX
• Version Model Number: 3650-24
• Company DUNS: 021129574
• Company Name: Litex Manufacturing, Inc.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060792970962 [Primary]

FDA Product Code

• FTA: Light, Surgical, Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-11
• Device Publish Date: 2025-08-01

Devices Manufactured by Litex Manufacturing, Inc.

• 00560792971716 - LITEX: 2025-08-11
• 05060792970009 - LITEX: 2025-08-11
• 05060792970016 - Litex: 2025-08-11
• 05060792970023 - LITEX: 2025-08-11
• 05060792970030 - LITEX: 2025-08-11
• 05060792970047 - Litex: 2025-08-11
• 05060792970054 - LITEX: 2025-08-11
• 05060792970061 - LITEX: 2025-08-11