Identity
- Trade Name
- BioPlex 2200 FDA UDI
- Generic Name
- Rubella virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- MMRV IgG Assay Protocol File CD, SW4.1_v1 FDA UDI
- Model / Reference
- SW4.1_V1 FDA UDI
- Description
- MMRV IgG Assay Protocol File CD, SW4.1_v1 FDA UDI
Identifiers
- Catalog Number
- 6652470D FDA UDI
- Primary DI / UDI-DI
- 00847865010979 FDA UDI
- FDA Product Code
- LJY FDA UDILFY FDA UDIOPL FDA UDILJB FDA UDI
- GMDN Term
- Rubella virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3380 FDA UDI866.3900 FDA UDI866.3510 FDA UDI866.3520 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Measles virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassayRubella virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassayMumps virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassayVaricella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
BioPlex 2200 by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BioPlex 2200 — Bio-Rad Laboratories · Class II
- BioPlex 2200 — Bio-Rad Laboratories · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
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
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 23210e39-ff87-4fea-be3f-f067d550b29a 36 fields · synced May 31, 2026