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Atellica CH C3

Siemens Healthcare Diagnostics Inc. · Model 11097624 · UDI-DI 00630414595665

CZW
1
510(k) clearances
3
Adverse events
1
Recalls
31
Facilities

Description

Complement C3 (C3) Atellica CH - RGT 400T

Recalls

DateFirmReason
2018-05-16Abbott Laboratories, IncAn update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.

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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.