Vascutek Limited

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Description

2 dispositivos en la base de datos

  • Modelo / Serial
    Catalogue Numbers: Biplex straight vascular grafts BL6006, BL6007,BL6008, BL6009, BL6010, BL6011, BL6012. BL6014.BL6016,BL4006, BL4008, BL3006, BL3007, BL3008, BL3009, BL3010, BL3011, BL3012, BL3014. 8L3016, Bl1506, BL1507, BL1508, BL1509, BL1510, BL1511, BL1512, BL1514, BL1516, BL5016.BL5018,BL5020j BL5022, BL5024, BL5026, Bl5028, BL5030, BL5032, BL5034, BL5036, BL5038, BL0526. BL0528, BL2518, BL2520, BL2522, BL2524, BL2526, BL2528, BL1218, BL1220, BL1222, BL1224, BL1226, BL1228. BL3018, BL3020, BL3022, BL3024, BL3026, BL3028, BL3030, BL3032, BL3034, BL3036, BL3038, BL1030, BL1032, BL1034, BL1036, Bl2030, BL2032, BL2034, BL2036, BL2038, BL4030, BL4032 Bt4034. BL4036, BL4038, BL6018, BL6020, BL6022, BL6024, BL6026, BL6028, BL6030, BL6032,BL6034. BL6036,BL6038 Biplex Valsalva vascular grafts BL0022ADP, BL0024ADP, BL0026ADP, BLO028ADP, BL0030ADP, BL0032ADP, Bl0034ADP Biplex Biovalsalva Conduit (stentless) EHVC21, EHVC23, EHVC25. EHVC27 . Stented Biovalsalva ~()nduit (Biplex stQl"ited) AHVC25, AHVC27, AHVC29 Batch No: All batches Serial No: All serial numbers
  • Descripción del producto
    Synthetic vascular graft and cardiac valve graft/vascular prosthesis, animal derived
  • Modelo / Serial
    -All Gelsoft™, Gelsoft Plus™, K-Thin, Gelsoft Plus™ ERS, K-Thin ERS, Gelseal™, Gelseal Plus™, Gelseal™ ERT and Gelweave™ Vascular Prostheses -All Thoraflex™ Hybrid Devices -All BioValsalva™ Stentless Biplex™ Conduits -All Stented BioValsalva™ Biplex™ Conduits -All RVOT elan™ Biplex™ Conduits Lot/Serial Number : All Lots
  • Descripción del producto
    Disposables

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Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
  • Empresa matriz del fabricante (2017)
  • Source
    MHSIDCCCDMIS
2 más