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IMMULITE®/IMMULITE® 1000 Systems TIE Total IgE

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Model 10380867 · UDI-DI 00630414966137

JHR
1
510(k) clearances
23
Adverse events
2
Recalls
6
Facilities

Description

IgE - IMMULITE - RGT - 100 Tests

Recalls

DateFirmReason
2013-12-20Siemens Healthcare DiagnosticsSiemens confirmed an overall average positive bias of 23% against the WHO 2nd IRP 75/502 with the IMMULITE Systems Total IgE assays.
2013-12-20Siemens Healthcare DiagnosticsSiemens confirmed an overall average positive bias of 23% against the WHO 2nd IRP 75/502 with the IMMULITE Systems Total IgE assays.

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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.