9 results · 6ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Metasul¿ LDH¿ Head Rx Sterile

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·November 14, 2012

Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.

FDA Enforcement
Class II ·Terminated·Welch Allyn Inc Mortara·April 28, 2021

smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·December 22, 2021

smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·December 22, 2021

Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 and 3HD012. An in vitro diagnostic multi-analyte calibrator for the calibration of Amylase (AMY), Gamma-Glutamyl Transferase (GGT), Lactate Dehydrogenase (LDH), Lipase (LIPL), and Pseudocholinesterase (PCHE) methods on the Dimension Vista System.

FDA Enforcement
Class II ·Terminated·Siemens Healthcare Diagnostics, Inc.·March 5, 2014

Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.

FDA Enforcement
Class II ·Terminated·Olympus Corporation of the Americas·August 14, 2019

Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019

Lactate Dehydrogenase L-P, (LDH) (NAO), Catalog Number LD3842 - Product Usage: device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum and plasma. This product is suitable for use on the RX series instruments which includes the RX daytona and RX imola.

FDA Enforcement
Class II ·Terminated·Randox Laboratories Ltd.·September 23, 2020

MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019