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ASI RPR Test for Syphilis for Use on the ASI Evolution
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- ASI RPR Test for Syphilis for Use on the ASI Evolution FDA UDI
- Generic Name
- Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI
- Device Name
- Syphilis Screening Test for Use on the ASI Evolution analyzer. 480 test kit FDA UDI
- Model / Reference
- NC-900480ABB FDA UDI
- Description
- Syphilis Screening Test for Use on the ASI Evolution analyzer. 480 test kit FDA UDI
Identifiers
- Catalog Number
- NC-900480ABB FDA UDI
- Primary DI / UDI-DI
- 00816057021673 FDA UDI
- FDA Product Code
- GMQ FDA UDI
- GMDN Term
- Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
Yes
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Treponema pallidum reagin antibody IVD, kit, agglutination
ASI RPR Test for Syphilis for Use on the ASI Evolution by Arlington Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Arlington Scientific, Inc.
Sources (1)
- FDA UDI 721cd12c-5b8a-4d8d-8cb7-9fb4420548f3 35 fields · synced Jul 18, 2026