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15,001 results

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Corrective Action for ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens PDF, 164KB, File does not meet accessibility standards Date: 21. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05195/12

Recall for ImmunoComb II HAV IgM, Orgenics PDF, 94KB, File does not meet accessibility standards Date: 21. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04813/12

Corrective Action for the HALOFLEX Energy Generator, BARRX Medical, Inc. PDF, 60KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05299/12

Safety Notice concerning the KleenSpec® Disposable Vaginal Specula, Welch Allyn Inc. PDF, 604KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - gynaecology
Reference 05373/12

Urgent Safety Notice for the use of the Agility™ and Apex™-Systems, Elekta PDF, 311KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 05160/12

Recall for LIFECODES PAK 12, PAKAUTO, PAKPLUS & PAK2-LE, Gen-Probe PDF, 2MB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05231/12

Recall of the power supply DT50 manufactured by Friwo and which is used with the Pari Sole N inhalation device, Pari GmbH PDF, 268KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - inhalation therapy
Reference 03411/11

Recall of the Symplicity® Catheter (Model RDN006), Medtronic PDF, 73KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05121/12

Recall for the Torque Wrench XIA3-Mantis Redux-Specialty Audible, Stryker Spine Bordeaux PDF, 37KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05349/12

Safety Notice for the Eclipse™ Treatment Planning System, Eclipse™ Treatment Planning System PDF, 292KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 05353/12