FDA Device Intelligence
HomeSiemens Healthcare Diagnostics Inc. › Atellica IM PCT

Atellica IM PCT

Siemens Healthcare Diagnostics Inc. · Model 10995651 · UDI-DI 00630414599694

NTM
3
510(k) clearances
8
Adverse events
2
Recalls
9
Facilities

Description

Procalcitonin (PCT) Atellica IM - RGT 100T

Recalls

DateFirmReason
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
2014-04-10Siemens Healthcare Diagnostics, IncSamples containing fluorescein may show interference with the ADVIA Centaur Systems TSH3 Ultra, Vitamin D and the ADVIA Centaur BRAHMS Procalcitonin assays.

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 docs
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.