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15,022 results

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Safety Notice for the product Ki67-MM1, Leica Biosystems PDF, 2MB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02312/15

Urgent Safety Notice for the product D-Dimer Gen.2, Roche Diagnostics PDF, 103KB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02420/15

Safety Information for the RELIANCE 4-FRONT single coil defibrillation leads, Boston Scientific Corporation PDF, 230KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 03051/15

Recall for the product Dermaroller MC, Dermaroller GmbH PDF, 3MB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - auxiliary equipment
Reference 02995/15

Corrective action for the HeartAttendant Interface Cable, ReliantHeart Inc. PDF, 31KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03037/15

Corrective action for the VenaSeal™ Closure System, Covidien Deutschland GmbH PDF, 152KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02675/15

Corrective action for the Philips Ultrasound EPIQ 7 Ultrasound System, Philips Healthcare - Ultrasound PDF, 292KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02875/15

Recall for DAT IgG-Dilution ID-Card, BioRad/DiaMed GmbH PDF, 1MB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02535/15

Safety Information for the product minisart (Exchange of mislabeled packages from lot 50057103), Sartorius Stedim Biotech GmbH PDF, 2MB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - filters
Reference 02001/15