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Atellica IM Tup

Siemens Healthcare Diagnostics Inc. · Model 10995712 · UDI-DI 00630414600253

KHQ
1
510(k) clearances
4
Adverse events
1
Recalls
33
Facilities

Description

T Uptake (Tup) Atellica IM - RGT 50T

Recalls

DateFirmReason
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.