768 results · 13ms · 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.

Reference Electrode Membranes for use with blood gas analyzer ABL 800 FLEX, when used on ABL 827 and ABL 837 with Creatinine modules (8x7). The device is packaged four (4) units per box.

FDA Recall
Terminated ·Radiometer America Inc·Product code CGL·March 26, 2009

ABL 5 Capillary Adaptor (a connection that fits the capillary tube on to the aspirator on the ABL 5 & BPH 5 Analyzers), in vitro diagnostic accessory, Part Number: 906-018.

FDA Recall
Terminated ·Radiometer America Inc·Product code CHL·June 9, 2005

Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal fixation device. 1)Screw Tower - REF 14-501660 2) Rod Reduce - REF 14-501661 3) Counter Torque - REF 14-501662

FDA Recall
Terminated ·Ebi, Llc·Product code LXH·August 13, 2013

BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system

FDA Recall
Terminated ·Ebi, Llc·Product code HWC·August 22, 2013

ARRAY and POLARIS Spinal System Medium Cross Connector Non Sterile Biomet Spine, Parsippany, NJ. 07054

FDA Recall
Terminated ·Ebi, Llc·Product code NKB·September 16, 2010

Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178

FDA Recall
Terminated ·Ebi, Llc·Product code HXX·September 29, 2012

Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Polaris Spinal System is a non-cervical, pedicle screw spinal fixation device.

FDA Recall
Terminated ·Ebi, Llc·Product code HXX·February 7, 2013

Shortened Plug Driver; Low Volume Specialty Device; Qty:1; Rx Only; Non Sterile; Biomet Spine, Parsippany, NJ 07054 The Polaris Spinal Systems is a non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion as a pedical screw fixation system, a posterior hook and sacral/iliac screw fixation system, or as an anterior or anterolateral fixation system. Pedicle screw fixation is limited to skeletal mature patients for use with autograft and/or allograft. The device is indicated for all the following indications:degenerative disc disease (defined as discogeneic back pain with degeneration of the disk confirmed by history and radiographic studies), spondylolisthesis, and or lordosis) tumor, stenosis, pseudoarthrosis, or failed previous fusion

FDA Recall
Terminated ·Ebi, Llc·Product code HXX·September 24, 2013

Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusion device.

FDA Recall
Terminated ·Ebi, Llc·Product code MAX·April 9, 2013

Cypher MIS Screw System-The system includes screws, various types and sizes of rods, and set screws. Various instruments are also available for use by the surgeon to facilitate implantation of the device. Non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion.

FDA Recall
Terminated ·Ebi, Llc·Product code NKB·October 8, 2014

Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Drill/Awl Sleeve Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.

FDA Recall
Terminated ·Ebi, Llc·Product code OVE·November 11, 2014

Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System.

FDA Recall
Terminated ·Ebi, Llc·Product code HXX·May 15, 2014

ABL 80 CO-OX SYSTEM, software versions 1.30 and 1.31 Additional Product Codes: CEM, CGA, CGZ, GHS, GKR, GLY, JFP, JGS, JIX, JJY, JPI The ABL 80 CO-OX SYSTEM is a portable, automated analyzer that measures pH, blood gases, electrolytes, glucose and oximetry in whole blood. The ABL 80 CO-OX SYSTEM is intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting.

FDA Recall
Terminated ·Sendx Medical Inc·Product code CHL·February 20, 2009

ANSPACH -4MM Carbide Fluted Ball, Extends 27MM; REF S-4BL-C-G1. Cutting shaping bone including spine and cranium.

FDA Enforcement
Class II ·Terminated·The Anspach Effort, Inc.·August 5, 2015

ABL 800 FLEX series blood gas analyzers containing software version 5.24.

FDA Recall
Terminated ·Radiometer America Inc·Product code CHL·November 13, 2006

ABL 700 Series blood gas analyzers equipped with Software Version 3.833.

FDA Recall
Terminated ·Radiometer America Inc·Product code CHL·November 13, 2006

Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzer, ABL-800 series.

FDA Recall
Terminated ·Radiometer America Inc·Product code CHL·June 17, 2005

Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzer, ABL-700 series.

FDA Recall
Terminated ·Radiometer America Inc·Product code CHL·June 17, 2005

BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system

FDA Enforcement
Class II ·Terminated·Ebi, Llc·November 27, 2013

Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Drill/Awl Sleeve Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·December 31, 2014