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

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Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98 Distal probe, labelled in green, consists of a 151kb probe distal to the NUP98 gene, covering the ZNF195 gene and the D11S4731 marker. Fluorescence in situ hybridisation (FISH) is a technique that allows the visualisation of DNA sequences upon chromosomes.

FDA Enforcement
Class II ·Terminated·Cytocell Ltd.·August 26, 2020

Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of two probes (71kb and 131kb) that are situated distal (telomeric) to the CRLF2 gene

FDA Enforcement
Class II ·Terminated·Cytocell Ltd.·February 17, 2021

CytoCell BCL11B Proximal in FITC Spectrum-LDT for investigation T-cell related malignancy. This device is an analyte specific reagent probe covering the 14q32.2 locus proximal to the BCL11B gene on chromosome 14. Ref: MPD39781

FDA Enforcement
Class II ·Terminated·Cytocell Ltd.·December 7, 2022

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

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

The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professional Nebulizer System is suitable for use in adult and pediatric patients. The Aeroneb Solo Nebulizer System is an iteration of the Aeroneb Professional Nebulizer System which is single patient use. The FRIWO AC/DC adapter is a component of the Aerogen Nebulizer systems which is used to power the Pro and Pro X controllers.

FDA Enforcement
Class II ·Terminated·Aerogen Ltd.·October 29, 2014

The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professional Nebulizer System is suitable for use in adult and pediatric patients. The Aeroneb Solo Nebulizer System is an iteration of the Aeroneb Professional Nebulizer System which is single patient use. The FRIWO AC/DC adapter is a component of the Aerogen Nebulizer systems which is used to power the Pro and Pro X controllers.

FDA Enforcement
Class II ·Terminated·Aerogen Ltd.·October 29, 2014

Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company

FDA Enforcement
Class II ·Terminated·Vascutek, Ltd.·August 27, 2014

Gelseal Straight Diameter 8mm Length 15cm. Vascular graft prosthesis is an implanted device intended to repair, replace, or bypass sections of native or artificial vessels, excluding coronary or cerebral vasculature, and to provide vascular access.

FDA Enforcement
Class II ·Terminated·Vascutek, Ltd.·July 8, 2015

Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).

FDA Enforcement
Class II ·Terminated·Lumenis Ltd·May 25, 2016

Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.

FDA Enforcement
Class II ·Terminated·Penlon, Ltd.·July 10, 2013

Inion GRT Tack, drill bit and tack appl., 4x, Sterile. Is indicated for the surgical treatment of periodontal defects to aid in the regeneration and integration of tissue components in guided tissue regeneration procedures, for pre-implant and peri-implant surgery and for covering bone defects and empty sockets.

FDA Enforcement
Class II ·Terminated·Inion Ltd.·March 22, 2017

Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator.

FDA Enforcement
Class II ·Terminated·ResMed Ltd.·June 17, 2015

Gelseal Straight Diameter 8mm Length 30cm. Vascular graft prosthesis is an implanted device intended to repair, replace, or bypass sections of native or artificial vessels, excluding coronary or cerebral vasculature, and to provide vascular access.

FDA Enforcement
Class II ·Terminated·Vascutek, Ltd.·July 8, 2015

The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professional Nebulizer System is suitable for use in adult and pediatric patients. The Aeroneb Solo Nebulizer System is an iteration of the Aeroneb Professional Nebulizer System which is single patient use. The FRIWO AC/DC adapter is a component of the Aerogen Nebulizer systems which is used to power the Pro and Pro X controllers.

FDA Enforcement
Class II ·Terminated·Aerogen Ltd.·October 29, 2014

The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professional Nebulizer System is suitable for use in adult and pediatric patients. The Aeroneb Solo Nebulizer System is an iteration of the Aeroneb Professional Nebulizer System which is single patient use. The FRIWO AC/DC adapter is a component of the Aerogen Nebulizer systems which is used to power the Pro and Pro X controllers.

FDA Enforcement
Class II ·Terminated·Aerogen Ltd.·October 29, 2014

NIO-A / NIO-P is an instant IO access device comprises housing with spring load mechanism that injects a trocar needle into the bone marrow of a patient and allows connection of syringe or IV administration set. The NIO-A is intended for adults above 12 years old and the NIO-P is intended for pediatric patients 3 - 12 years of age.

FDA Enforcement
Class II ·Terminated·Waismed Ltd·September 7, 2016

Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component.

FDA Enforcement
Class II ·Terminated·Corin Ltd·June 23, 2021