Identity
- Trade Name
- BioPlex 2200 FDA UDI
- Generic Name
- Treponema pallidum reagin antibody IVD, reagent FDA UDI
- Device Name
- BioPlex 2200 Syphilis Total & RPR Assay Protocol File CD SW4.3_v1 FDA UDI
- Model / Reference
- 4.3_v1 FDA UDI
- Description
- BioPlex 2200 Syphilis Total & RPR Assay Protocol File CD SW4.3_v1 FDA UDI
Identifiers
- Catalog Number
- 12000657 FDA UDI
- Primary DI / UDI-DI
- 03610520138267 FDA UDI
- FDA Product Code
- LIP FDA UDIGMQ FDA UDI
- GMDN Term
- Treponema pallidum reagin antibody IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3830 FDA UDI866.3820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Treponema pallidum total antibody IVD, kit, fluorescent immunoassayTreponema pallidum reagin antibody IVD, reagent
BioPlex 2200 by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Treponema pallidum reagin antibody IVD, reagent.
- BioPlex 2200 — Bio-Rad Laboratories · Class II
- BioPlex 2200 — Bio-Rad Laboratories · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI f2122946-3790-47cd-9c9c-c28fc287bf45 36 fields · synced May 31, 2026