Thompson Surgical Instruments Flatmat 25" 40029

GUDID 00812432022426

LUMITEX, INC.

Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light

• Primary Device ID: 00812432022426
• NIH Device Record Key: d6f425ae-8173-48a7-8408-a9579eb14ca1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thompson Surgical Instruments Flatmat 25"
• Version Model Number: 012525
• Catalog Number: 40029
• Company DUNS: 108631797
• Company Name: LUMITEX, 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812432022426 [Primary]

FDA Product Code

• FDG: Retractor, Fiberoptic

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: 2021-03-29
• Device Publish Date: 2021-03-19

Devices Manufactured by LUMITEX, INC.

• 00812432023010 - Thompson Surgical Instruments Lite Path Integrated Double 13mm: 2023-11-09
• 00812432022396 - Spineart Wolf Cable Adaptor: 2023-08-21
• 00812432022921 - Spineart Olympus Cable Adaptor: 2023-08-21
• 00810025485344 - MiRus Bifurcated Illuminator: 2023-08-21
• 00812432021559 - Spineart Storz Cable Adaptor: 2023-08-21
• 00812432021689 - Lumitex 4mm Universal Fiber Optic Cable: 2023-08-21
• 00812432021696 - Lumitex 3.5mm Fiber Optic Cable: 2023-08-21
• 00812432022655 - Orthofix Surgical Illuminator: 2023-08-21