Elecsys Anti-Tg 09005021190

GUDID 07613336171479

Roche Diagnostics GmbH

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• Primary Device ID: 07613336171479
• NIH Device Record Key: 08f51881-fc1d-467d-98bd-133019343ae5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elecsys Anti-Tg
• Version Model Number: 09005021190
• Catalog Number: 09005021190
• 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	07613336171479 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222610

FDA Product Code

• JZO: SYSTEM, TEST, THYROID AUTOANTIBODY

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 Anti-Tg]

• 07613336203521: 09004998160
• 07613336171479: 09005021190