Identity
- Trade Name
- MAS Syphilis Positive Control FDA UDI
- Generic Name
- Treponema pallidum total antibody IVD, control FDA UDI
- Model / Reference
- 10027483 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884883007536 FDA UDI
- FDA Product Code
- OHQ FDA UDI
- GMDN Term
- Treponema pallidum total antibody IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
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 total antibody IVD, control
MAS Syphilis Positive Control by Microgenics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Treponema pallidum total antibody IVD, control.
- Atellica IM Syph QC — Siemens Healthcare Diagnostics · Class II
- Alinity — Abbott · Class I
- Syphilis Control — Fujirebio Diagnostics, Inc. · Class I
- PreciControl Release Syphilis — Roche Diagnostics Corp. · Class I
- Trinity Biotech — MARDX DIAGNOSTICS, INC. · Class II
- LIAISON® Treponema Serum Controls — Diasorin Inc.
- VIROTROL — Bio-Rad Laboratories · Class I
- ARCHITECT — Abbott · Class II
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 I | Pending data |
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Manufacturer
- Manufacturer
- Microgenics Corporation
Sources (1)
- FDA UDI 302891b2-334e-4518-adeb-c217cb6a7c72 32 fields · synced Jun 9, 2026