8 results · 15ms · 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.

FSE Image Upgrade Kit, Catalog # 92019C This kit is used to install and/or upgrade software used with the EVOLIS Microplate System.

FDA Enforcement
Class III ·Terminated·Bio-Rad Laboratories·October 30, 2013

The spare component Anti-HBs Cutoff Calibrator, 10 mLU/mL, Catalog number 26154. The spare component is sold separately from the MONOLISA Anti-HBs EIA Kit contains an expiration date of 2016-04-30 in error.

FDA Enforcement
Class III ·Terminated·Bio-Rad Laboratories, Inc.·July 1, 2015

Liquichek" ToRCH Plus IgM Control - Positive Liquichek ToRCH Plus IgM Control is intended for use as an unassayed quality control serum to monitor precision of IgM laboratory testing procedures for the analytes listed in this package insert. This product is not intended for use in blood donor screening assays. Analytes claimed with this lot of Liquichek ToRCH Plus IgM Control: ¿ Cytomegalovirus (CMV) IgM ¿ Herpes Simplex Virus Type 1/2 (HSV-1/2) IgM ¿ Rubella Virus IgM ¿ Toxoplasma gondii IgM

FDA Enforcement
Class III ·Terminated·Bio-rad Laboratories, Inc.·May 22, 2013

D-10 Dual Program, which contains Update Kit D-10 A1c program diskette. United States; Bio-Rad Laboratories, Hercules, CA 94547 The Bio-Rad D-10 Hemoglobin Testing System provides an integrated method for the separation and determination of the relative percent of specific hemoglobins (e.g., A2, F, Ale} in whole blood. The separation is based on the principles of high performance liquid chromatography.

FDA Enforcement
Class III ·Terminated·Bio-Rad Laboratories, Inc.·February 19, 2014

Flyte Togas are components of the Stryker Flyte System and are intended to be worn over any Stryker Flyte Helmet. This toga provides Level 1 and 4 protection according to the Association for the Advancement of Medical Instrumentation (AAMI) Liquid Barrier Performance and Classification System (PB70:2012).

FDA Enforcement
Class III ·Terminated·Stryker Instruments Div. of Stryker Corporation·February 18, 2015

Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and provide power to non-sterile and sterile batteries. The Stryker Universal Battery Charger is a four station, modular battery charger intended to charge Stryker handpiece battery packs only. The battery charger has the optional functionality to track device usage data. Usage data is accumulated by Stryker and reports are able to be provided to the customer. For powered surgical instruments.

FDA Enforcement
Class III ·Terminated·Stryker Instruments Div. of Stryker Corporation·May 13, 2015

RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

FDA Enforcement
Class III ·Terminated·Stryker Instruments Div. of Stryker Corporation·November 23, 2016

Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6

FDA Enforcement
Class III ·Terminated·Stryker Instruments Div. of Stryker Corporation·July 27, 2022