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15,013 results

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Corrective action for the VERO™/MHI-TM2000 Linear Accelerator System, Mitsubishi Heavy Industries, Ltd. PDF, 3MB, File does not meet accessibility standards Date: 29. July 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03965/14

Corrective action for the KODAK DirectView DR 7500 System, Carestream Health, Inc. PDF, 21KB, File does not meet accessibility standards Date: 29. July 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03976/14

Corrective action for the diagnostic ultrasound system ARIETTA 60 and ARIETTA 70, Hitachi Aloka Medical, Ltd. PDF, 101KB, File does not meet accessibility standards Date: 29. July 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 03746/14

Corrective action for the Recipient Vacuum Trephine, Network Medical Products PDF, 354KB, File does not meet accessibility standards Date: 29. July 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04300/14

Corrective action for certain care beds from Hermann Bock GmbH / Replacement of MD201 twin drives from limoss GmbH & Co. KG PDF, 195KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 03800/14

Corrective action concerning the ACL TOP Family Coagulation Systems, Instrumentation Laboratory PDF, 45KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03699/14

Corrective action for the ADVIA Centaur® CP, Siemens PDF, 36KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03728/14

Safety Notice for the PTFE Ventilation Tubes, Spiggle & Theis Medizintechnik GmbH PDF, 12MB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03373/14

Urgent Safety Notice for the E.CAM® Patient Handling System (PHS), Siemens PDF, 483KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 04242/14

Recall for the FOCUS Gesundheit Kinderwunsch-Test, ulti med Products (Deutschland) GmbH PDF, 213KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00830/13