Elecsys Tg II 08906556160

GUDID 07613336203569

Roche Diagnostics GmbH

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• Primary Device ID: 07613336203569
• NIH Device Record Key: 5fd6bdb3-b6cf-4c95-ad64-1d0209c83aa6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elecsys Tg II
• Version Model Number: 08906556160
• Catalog Number: 08906556160
• Company DUNS: 315028860
• Company Name: Roche Diagnostics GmbH
• 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: true
• 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	07613336203569 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221890

FDA Product Code

• MSW: System, test, thyroglobulin

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: 2023-11-08
• Device Publish Date: 2023-10-31

On-Brand Devices [Elecsys Tg II]

• 07613336203569: 08906556160
• 07613336169582: 08906564190