Yumizen T6000

GUDID 03610230008959

Right module 2 Inst

HORIBA ABX SAS

Belt conveyor

• Primary Device ID: 03610230008959
• NIH Device Record Key: b913aa6e-2d6b-4c0e-8d69-b819ba392499
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Yumizen T6000
• Version Model Number: 1300059861
• Company DUNS: 273647420
• Company Name: HORIBA ABX SAS
• 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: 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	03610230008959 [Primary]

FDA Product Code

• LXG: Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

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: 2024-06-07
• Device Publish Date: 2024-05-30

On-Brand Devices [Yumizen T6000]

• 03610230008959: Right module 2 Inst
• 03610230008942: Right module 1 Inst back
• 03610230008935: Right module Inst only
• 03610230008928: Right module SPS only