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Radioassay, Triiodothyronine Uptake

FDA product code KHQ · Class 2 · Clinical Chemistry

28
Registered devices
4
Adverse events
1
Recalls
93
510(k) clearances

Devices with this code

CEDIA T Uptake — Microgenics CorporationElecsys Tuptake Assay — Roche Diagnostics GmbHAIA-PACK T-U CALIBRATOR SET — TOSOH CORPORATIONDRI T-Uptake Calibrator Kit — Microgenics CorporationARCHITECT — ABBOTT LABORATORIEST3 Uptake 125I RIA Kit — MP BIOMEDICALS, LLCAlinity — Abbott Ireland DiagnosticsT3 Uptake 125I RIA 200 Tube Kit — MP BIOMEDICALS, LLCT3 Uptake AccuLite CLIA Test System - 192 Wells — MONOBIND, INC.Dimension® Flex® reagent cartridge TU — Siemens Healthcare Diagnostics Inc.T3 Uptake AccuLite CLIA Test System - 96 Wells — MONOBIND, INC.ADVIA Centaur® Tup — Siemens Healthcare Diagnostics Inc.T3-Uptake ELISA — DRG International IncST AIA-PACK T-U — TOSOH CORPORATIONElecsys T-Uptake — Roche Diagnostics GmbHDRI T-Uptake — Microgenics CorporationVITROS — ORTHO CLINICAL DIAGNOSTICSDimension Vista® Flex® reagent cartridge TU — Siemens Healthcare Diagnostics Inc.Atellica IM Tup — Siemens Healthcare Diagnostics Inc.T3 Uptake AccuBind ELISA Test System - 96 Wells — MONOBIND, INC.TUptake — Roche Diagnostics GmbHVITROS — ORTHO CLINICAL DIAGNOSTICSiFlash-FT3 — Shenzhen YHLO Biotech Co., Ltd.T3-Uptake ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung

Recent 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, dependin

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.