Home › Siemens Healthcare Diagnostics Inc. › Atellica IM Tup
Atellica IM Tup
Siemens Healthcare Diagnostics Inc. · Model 10995712 · UDI-DI 00630414600253
1
510(k) clearances
4
Adverse events
1
Recalls
33
Facilities
Description
T Uptake (Tup) Atellica IM - RGT 50T
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-05 | Tosoh Bioscience Inc | Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay. |
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.
