Home › EUROIMMUN Medizinische Labordiagnostika AG › Anti-M2-3E ELISA (IgG)
Anti-M2-3E ELISA (IgG)
EUROIMMUN Medizinische Labordiagnostika AG · Model EA 1622-9601 G · UDI-DI 04049016027157
1
510(k) clearances
1
Adverse events
2
Recalls
17
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-07-29 | Bio-Rad Laboratories | The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit. |
| 2004-04-12 | Diasorin Inc. | The data reduction program written for a specific automated microtiter plate instrument (Bio-Tek ELx800 reader) was found to be faulty. This program is used to calculate the cut o |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
