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14,979 results

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Safety Notice for SYNCHRON UniCel DxC Clinical Systems - Tube Assembly 142, Beckman Coulter PDF, 40KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02839/09

Follow-up Notice for AED Plus Defibrillator, Zoll PDF, 130KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00668/09

Safety Information for AvantGuard 1600 beds - AvantGuard Li160A, Hill-Rom PDF, 40KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01209/09

Recall for Factor V Leiden Kit, Roche PDF, 37KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02619/09

Corrective action for HeartStart MRx, Philips PDF, 186KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02693/09

Safety Notice for Aesculap cementless Bicontact N stem size 9, Aesculap AG PDF, 64KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02733/09

Safety Notice for Separator 032 - Penumbra System, Penumbra Inc. PDF, 56KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02751/09

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