Yumizen C1200 Rheumatoid Factor

GUDID 03610230007402

HORIBA ABX SAS

Rheumatoid factor IVD, kit, nephelometry/turbidimetry

• Primary Device ID: 03610230007402
• NIH Device Record Key: 51da55a8-a884-4a79-aae1-d8068de742ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Yumizen C1200 Rheumatoid Factor
• Version Model Number: 1300023888
• Company DUNS: 273647420
• Company Name: HORIBA ABX SAS
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03610230007402 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191562

FDA Product Code

• DHR: System, Test, Rheumatoid Factor

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: 2020-05-14
• Device Publish Date: 2020-05-06

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• 03610230009451 - Yumizen H2500: 2024-12-09
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