Imager Adaptor for SeaSpine® Lattus Retractor

GUDID 00850007069582

Imager Adaptor for SeaSpine® Lattus Retractor, 5-pk Carton

VISEON, INC.

General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope General-purpose surgical microscope

• Primary Device ID: 00850007069582
• NIH Device Record Key: e9d12c85-4438-446f-9f42-1f595781c6f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Imager Adaptor for SeaSpine® Lattus Retractor
• Version Model Number: LTS-S
• Company DUNS: 096680671
• Company Name: VISEON, INC.
• Device Count: 5
• 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: true
• 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	00850007069582 [Unit of Use]
GS1	00850007069612 [Primary]

FDA Product Code

• FSO: Microscope, Surgical, General & Plastic Surgery

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: 2024-02-13
• Device Publish Date: 2024-02-05

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