Identity
- Trade Name
- BioPlex 2200 FDA UDI
- Generic Name
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, control FDA UDI
- Device Name
- BioPlex 2200 ToRC IgM Control Lot Data FDA UDI
- Model / Reference
- 12000673 FDA UDI
- Description
- BioPlex 2200 ToRC IgM Control Lot Data FDA UDI
Identifiers
- Catalog Number
- 12000673 FDA UDI
- Primary DI / UDI-DI
- 03610520269541 FDA UDI
- FDA Product Code
- JJX FDA UDI
- GMDN Term
- Toxoplasma gondii immunoglobulin M (IgM) 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
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: Rubella virus immunoglobulin M (IgM) antibody IVD, controlToxoplasma gondii immunoglobulin M (IgM) antibody IVD, controlCytomegalovirus (CMV) immunoglobulin M (IgM) antibody IVD, control
BioPlex 2200 by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cytomegalovirus (CMV) immunoglobulin M (IgM) antibody IVD, control.
- CMV Negative Control — BION ENTERPRISES, LTD. · Class II
- LIAISON CMV IgM Serum Control Set — Diasorin Inc.
- PreciControl CMV IgM — Roche Diagnostics Corp. · Class I
- CMV IgM Control — BION ENTERPRISES, LTD. · Class II
- LIAISON® Control CMV IgM — Diasorin Inc.
- BioPlex 2200 — Bio-Rad Laboratories · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 34110380-a61b-46ce-ac7e-b368bc5b9c66 36 fields · synced Jun 1, 2026