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14,979 results

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Recall for the Firebird Spinal Fixation System Modular Screwdriver, Orthofix PDF, 391KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07170/13

Safety Information for Elekta Precise Tables™ range 124001 to 126924, 133801 to 133999, 213000 to 213398, 227001 to 227144. PDF, 406KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - others
Reference 01324/13

Second Safety Notice for the Cadisc™-C Endplate Handles and Blades, Ranier Technology Limited PDF, 210KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07151/12

Safety Notice for the HeartStart FRx or HeartStart HS1 automated external defibrillators (AEDs), Philips Healthcare PDF, 47KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07471/13

Safety Notice for all 3DLINE DMLC systems on an Elekta digital accelerator, Elekta PDF, 256KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 04902/13

Safety Notice for DMLC systems on an Elekta digital accelerator, Elekta PDF, 257KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 04902/13

Corrective action for BBL MGIT Mycobacteria Growth Indicator Tubes, Becton Dickinson PDF, 59KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05503/13

Safety Notice for overhead Video Monitor Suspension of Precision 500D, Legacy, Prestilix, Monitrol, RFX, SFX, Tilt-C, Prestige VH, Prestige SI and Prestige SII X-ray systems, GE Healthcare PDF, 89KB, File does not meet accessibility standards Date: 13. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07171/13

Safety Notice concerning EPIQ 7 Ultrasound systems with software version 1.0 and 1.0.1, Philips Healthcare PDF, 57KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 06749/13

Recall for Alere Triage® Troponin I,Alere PDF, 62KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06837/13

Corrective Action for the ABL90FLEX Analyzers, Radiometer PDF, 30KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06492/13

Recall of BD Sabouraud Agar with Gentamycin and Chloramphenicol, Becton Dickinson PDF, 73KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06636/13

Recall for i-STAT PT/INR cartridge, Abbott PDF, 57KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06512/13

Recall of several lots of COBE® Spectra Apheresis System Disposable tubing sets FSN BCT8, Terumo PDF, 100KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 05955/13

Corrective action for the BFT II Analyzer, Siemens PDF, 25KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06653/13

Safety Notice for upcoming safety inspection for Symbia E- or e.cam-system, Siemens Healthcare PDF, 74KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06686/13

Lot Recall of the NX3 Try-In Gel, KERR PDF, 182KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 05568/13

Safety Notice for the IntelliSpace PACS system, Philips Healthcare PDF, 440KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 06700/13

Safety Notice for Artis biplane system, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 07112/13

Safety Notice for ConMed Electrosurgery ALTRUS® Termal Tissue Fusion Handpieces (2 lots), ConMed Corporation PDF, 65KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06493/13