ARTHREX

GUDID 00195174067154

LG Electronics Inc.

Image display unit, colour

• Primary Device ID: 00195174067154
• NIH Device Record Key: 4c225d2c-ae2f-4742-a9a8-bd7d606b2b7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARTHREX
• Version Model Number: AR-3250-3212
• Company DUNS: 688298116
• Company Name: LG Electronics 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	00195174067154 [Primary]

FDA Product Code

• FWB: Camera, Television, Surgical, Without Audio

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: 2023-06-27
• Device Publish Date: 2023-06-19

Devices Manufactured by LG Electronics Inc.

• 08806096660263 - LG: 2025-09-29
• 00195174123508 - LG: 2025-08-01
• 00195174123515 - LG: 2025-08-01
• 00195174113950 - LG: 2025-02-21
• 00195174113875 - LG: 2025-01-16
• 00195174112779 - LG: 2024-12-23
• 00195174080269 - LG: 2024-09-06
• 00195174099452 - LG: 2024-08-02