ZedView

GUDID 14573443600029

LEXI CO., LTD.

Orthopaedic/craniofacial implantation planning software

• Primary Device ID: 14573443600029
• NIH Device Record Key: 5f43de13-073b-4cba-9b7f-2ce852d43376
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZedView
• Version Model Number: Ver.14.0.4.1
• Company DUNS: 697449465
• Company Name: LEXI CO., LTD.
• 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: 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

Customer Support Contacts

• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +810353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp
• Phone: +81353944833
• Email: lexi_global@lexi.co.jp

Device Identifiers

Device Issuing Agency	Device ID
GS1	14573443600029 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200704

FDA Product Code

• LLZ: System, Image Processing, Radiological

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: 2022-01-04
• Device Publish Date: 2021-12-27