Access Syphilis Reagent C80411

GUDID 15099590763626

The Access Syphilis assay is a paramagnetic particle, chemiluminescent immunoassay for the qualitative detection of total antibodies to Treponema pallidum in human serum and plasma using the Access Immunoassay Systems. It is intended to be used as an aid in the diagnosis of syphilis or in conjunction with a nontreponemal laboratory test and clinical findings to aid in the diagnosis of syphilis infection. The Access Syphilis assay is not intended for blood and tissue donor screening.

Beckman Coulter, Inc.

Treponema pallidum total antibody IVD, kit, chemiluminescent immunoassay

• Primary Device ID: 15099590763626
• NIH Device Record Key: 7ef0b4d3-fbec-4bf6-b2d1-61a9d968dbcf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Access Syphilis Reagent
• Version Model Number: C80411
• Catalog Number: C80411
• Company DUNS: 008254708
• Company Name: Beckman Coulter, Inc.
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	15099590763626 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241427

FDA Product Code

• LIP: Enzyme Linked Immunoabsorption Assay, Treponema Pallidum

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: 2025-05-15
• Device Publish Date: 2025-05-07

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