MTI

GUDID 06974570910011

Material Technology Innovations Co., Ltd.

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• Primary Device ID: 06974570910011
• NIH Device Record Key: 22c4673e-9a2c-4e4d-a408-cead53dc4cbf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MTI
• Version Model Number: T02
• Company DUNS: 544467122
• Company Name: Material Technology Innovations Co., Ltd.
• 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: true
• 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	06974570910011 [Primary]

FDA Product Code

• EJH: Alloy, Metal, Base

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: 2023-04-07
• Device Publish Date: 2023-03-30

On-Brand Devices [MTI]

• 06974570910028: C02-A
• 06974570910011: T02
• 06974570910004: C01-A