105 results · 8ms · Sources: EU EUDAMED, US FDA

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N Latex CDT Kit

FDA Enforcement
Class II ·Terminated·CSL Behring GmbH·September 5, 2018

Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity , Adt/Pedi Intub CO2 Line LTerm Lng , Adt/Pedi Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line High Humidity , Neo/Inf Intub CO2 Line LTerm Lng , VitaLine H Set Adult/Pediatric , VitaLine H Set Infant/Neonatal , FilterLine Set Long Adult/Pediatric , FilterLine H Set Long Adult/Pediatric , FilterLine H Set Long Infant/Neonatal , Trade Compliant: FilterLine H, Adult/Ped , Trade Compliant: FilterLine H, Infant/Neo , FilterLine Set Adult/Pedi , FilterLine H Set Adult/Pedi and FilterLine H Set Infant/Neonatal. Carbon dioxide gas analyzer.

FDA Enforcement
Class II ·Ongoing·Philips North America Llc·May 14, 2025

Siemens N Latex CDT Kit- IVD quantitative determination of carbohydrate-deficient transferrin (CDT) in human serum. Siemens Material Number (SMN): 10445997

FDA Enforcement
Class II ·Terminated·CSL Behring GmbH·April 29, 2020

Cobalt XT HF CDT-D MRI SureScan, Model Number: DTPA2D4, Implantable Cardioverter Defibrillator

FDA Enforcement
Class II ·Ongoing·Medtronic Inc.·July 3, 2024

Merge OrthoPACS software. The firm name on the label is Merge Healthcare, Hartland, WI.

FDA Enforcement
Class II ·Terminated·Merge Healthcare, Inc.·June 28, 2017

Merge PACS software. The firm name on the label is Merge Healthcare.

FDA Enforcement
Class II ·Terminated·Merge Healthcare, Inc.·March 15, 2017

CHS Custom Convenience Kit- (1) DT SCATPAD, DBL. TAPE, 12.5 X 16.5 Product Number: SEPA 402 (2) SCATPAD, 11 X 34 Product Number: SPA502

FDA Enforcement
Class II ·Terminated·Custom Healthcare Systems, Inc.·October 31, 2018

LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996-000515 Masimo¿ LNCS-II rainbow¿ DCI 8¿ SpCO, Adult Reusable Sensor REF 11996-000519 Masimo¿ LNCS-II rainbow¿ DCI 8¿ SpCO, Pediatric Reusable Sensor REF 11996-000520 The LIFEPAK¿ 15 Monitor/Defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. RD rainbow" 8¿ SpCO sensors are indicated for the continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO¿), and methemoglobin saturation (SpMet¿) for use with adult, pediatric, infant, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused in hospitals, hospital-type facilities, mobile, and home environments.

FDA Enforcement
Class II ·Ongoing·Physio-Control, Inc.·February 26, 2025

The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative, multiplexed in vitro diagnostic test for the rapid detection of toxin A (tcdA), toxin B (tcdB), and tcdC gene sequences of toxigenic strains Clostridium difficile and for presumptive identification of PCR ribotype 027 strains from unformed (liquid or soft) stool specimens collected from patients suspected of having C. difficile infection (CDI). Presumptive identification of the PCR ribotype 027 strain of C. difficile is by detection of the binary toxin (cdt) gene sequence and the single base pair deletion at nucleotide 117 in the tcdC gene. The tcdC gene encodes for a negative regulator in C. difficile toxin production. The test is performed on the Verigene System and utilizes automated specimen preparation and polymerase chain reaction (PCR) amplification, combined with a nanoparticle-based array hybridization assay to detect the toxin gene sequences associated with toxin-producing C. difficile.

FDA Enforcement
Class II ·Terminated·Nanosphere, Inc.·October 1, 2014

Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process laboratory data.

FDA Enforcement
Class II ·Terminated·Roche Diagnostics Operations, Inc.·September 10, 2014

Food Intolerance Test Small

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Lactose Intolerance Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Mycotoxin Panel Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Fructose Intolerance Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Intestinal Worms Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Iodine Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Menopause (FSH) 2 Tests

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Biological Age & Longevity Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Iron Deficiency Test (ferritin)

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025

Men s Hormone Test

FDA Enforcement
Class II ·Ongoing·GET TESTED INTERNATIONAL AB·December 10, 2025