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14,979 results

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Urgent Safety Notice for IsoSeed and IsoCord, Eckert & Ziegler BEBIG, Berlin PDF, 65KB, File does not meet accessibility standards Date: 04. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - implantats emitting radioactive radiation
Reference 07913/12

Urgent Safety Notice regarding implantable HeartWare Ventricular Assist System (VAS), HeartWare Inc. PDF, 124KB, File does not meet accessibility standards Date: 04. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 00883/13

Recall Information: Curapor transparent, Curafix i.v. control and Raucodrape Inzisionsfolie, Lohmann & Rauscher PDF, 745KB, File does not meet accessibility standards Date: 01. March 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - bandages
Reference 00910/13

Safety Notice for the ACUSON S2000 Automated Breast Volume Scanner, Siemens PDF, 106KB, File does not meet accessibility standards Date: 20. February 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00484/13

Lot Recall for ALLEVYN Cavity Wound 5 cm circular, Smith & Nephew PDF, 103KB, File does not meet accessibility standards Date: 18. February 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 00603/13

Safety Information for octenilin Wound Gel, octenilin Wound Irrigation Solution and octenisept Wound Gel, Schülke & Mayr PDF, 1MB, File does not meet accessibility standards Date: 12. February 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - ointments and gels
Reference 00208/13

Safety Notice concerning a software update required on Sonalleve MR-HIFU Therapy System with R3.1 and R3.2 application software PDF, 47KB, File does not meet accessibility standards Date: 12. February 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic therapeutic equipment
Reference 00562/13

Lot Recall of the LAPRA-TY-II CLIP, PDS II, Vicryl, Vicryl Plus, Ultrapro, Ultrapro Plug, Vicryl Meshes, Johnson & Johnson PDF, 338KB, File does not meet accessibility standards Date: 05. February 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 00455/13

Safety Notice for ISOLINE defibrillation leads, Sorin Group Italia Srl PDF, 45KB, File does not meet accessibility standards Date: 05. February 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 00433/13

Urgent Safety Notice for NAVIOS™ Flow Cytometer, Beckman Coulter PDF, 231KB, File does not meet accessibility standards Date: 30. January 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00119/13

Safety Notice for Video-Duodenoscope TJF-Q180V, Olympus PDF, 739KB, File does not meet accessibility standards Date: 25. January 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 00239/13

Safety Notice concerning the Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall®, Multirall® and Masterlift® Systems, Liko PDF, 811KB, File does not meet accessibility standards Date: 24. January 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 00220/13

Safety Notice for OEC Uroview X-Ray system, GE Healthcare PDF, 1MB, File does not meet accessibility standards Date: 24. January 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03227/06

Safety Notice for the product AutoTac Delivery Handle und AutoTac Titanium Starter Kit, BIOHORIZON IMPLANT SYSTEMS PDF, 34KB, File does not meet accessibility standards Date: 15. January 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 07542/12

Safety Notice and Recall of Lithium Ion Polymer Batteries used as componets of Companion Driver Systems, Syncardia Systems Inc. PDF, 126KB, File does not meet accessibility standards Date: 11. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 07652/12

Safety Notice for application and recall of DBS Extensions Kits PDF, 94KB, File does not meet accessibility standards Date: 09. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 07585/12

Safety Notice on pacemakers (Models Accent SR PM1110 and Accent DR PM2112), St. Jude Medical PDF, 235KB, File does not meet accessibility standards Date: 04. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 07477/12

Lot Recall of STERRAD® NX® System Cassettes REF 10133, ASP PDF, 44KB, File does not meet accessibility standards Date: 03. January 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 07558/12

Recall for Antimicrobial Susceptibility Testing Disc, Oxoid PDF, 17KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07555/12

Lot Recall of TRIGEN INTERTAN nails, SMITH & NEPHEW PDF, 97KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07646/12