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14,962 results

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Recall for INNOTEST hPLAP, INNOGENETICS PDF, 46KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02600/09

Recall for intragastric balloons HELIOSPHERE, HELIOSCOPIE PDF, 72KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02265/09

Corrective Action for EasyLink Informatics System, Siemens Healthcare PDF, 24KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02617/09

Recall for Stryker PainPump Catheters, Stryker GmbH PDF, 112KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02602/09

Recall for Hintegra saw blade 60° AO-Synthes, Newdeal PDF, 164KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02312/09

Recall for HemaCarotid Patch ultrathin knitted, InterVascular S.A.S. PDF, 73KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02542/09

Safety Notice for Targon PFT System - KH 535 R, Aesculap PDF, 107KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02791/09

Information for Super Elastic Self-Crimping Nitinol Piston, AUDIO TECHNOLOGIES PDF, 141KB, File does not meet accessibility standards Date: 11. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02249/09

Safety Notice for Signa 3T Magnetic Resonance Systems, GE Healthcare PDF, 64KB, File does not meet accessibility standards Date: 11. August 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 01628/08

Recall for BHR Acetabular Cups, Smith & Nephew PDF, 663KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02307/09

Recall for GALILEO Cervical Disc Prosthesis, SIGNUS MEDIZINTECHNIK GmbH PDF, 168KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02712/09

Recall for 4Z1c Matrix Array Transducer on the ACUSON SC2000, Siemens PDF, 78KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02706/09

Safety Notice for Angiostar, Multistar, Neurostar, Coroskop and Bicor systems, Siemens PDF, 491KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01303/09

Recall for Twin-Pass® Dual Access Catheter, Vascular Solutions PDF, 125KB, File does not meet accessibility standards Date: 07. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02538/09

Safety Notice for Hedrin, Pouxit, Silikom, Etopril and XT Luis, Thornton & Ross PDF, 88KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 04774/08

Recall for PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences PDF, 137KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04519/08

Safety Notice for Centricity PACS RA1000 Workstation; Software: 2.1.x and 3.0.x, GE Healthcare PDF, 142KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Safety Notice for Centricity PACS RA1000 Workstation; Software: PathSpeed 7.x, 8.x, Centricity 1.X, 2.0.X, GE Healthcare PDF, 142KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Safety Notice for Centricity PACS RA1000 Workstation Software, GE Healthcare PDF, 76KB, File does not meet accessibility standards Date: 04. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09