Etest Colistin

  • Modelo / Serial
    1004970070, 1004872780, 1004861970, 1004832200, || 1004752300, 1004606550, 1004523860, 1004464760, || 1004437930, 1004386240, 1004329220, 1004260630, || 1004190730, 1004171220, 1004129560, 1004070260, || 1003969990, 1003940910, 1003890030, 1003767080 || 1003725600, 1003643960, 1003610660, 1003532330, || 1003514810, 1003409250, 1003297790, 1003240130, || 1003146250, 1003105550 1003052570, 1002894460, || 1002849110, 1002816570, 1002807980, 1002780680, || 1002718610, 1002594030, 1002438560, 1002336190, || 1002280740, 1002154530, 1002106970, 1002053380, || 1001988910, 1001920000, 1001898050, 1001742150 || 1001721800,1001687660, 1001596380, 1001567710 || 1001496190, 100149600, 1001472220, 1001417080, || 1001338240, 1001317190 1001260560, 1001158900, || 1001142860, 1001032680, 1001062860, 1000941970, || 1000893880, 1000756330, 1000750130, 1000746340 || 1000714690, 1000651250, 1000635770, 1004972220, || 1004864570, 1004791040, 1004752310, 1004596710, || 1004595380, 1004542160 1004520890, 1004442040, || 1004439600, 1004329200, 1004235390, 1004177660, || 1004131970, 1004075130, 1003995330, 1003946110 || 1003767090, 1003728970, 1003616140, 1003532390, || 1003456440, 1003403320, 1003205800, 1002989530, || 1002889130, 1002795210 1002781850, 1002703940, || 1002598660, 1002523000, 1002343060, 1002273500, || 1002123120, 1002019070, 1002019130, 1001965280 || 1001744750, 1001721810, 1001707310, 1001634590, || 1001548430, 1001548440, 1001456040, 1001417090, || 1001307480, 1001307490 1001200010, 1001183170, || 1001158910, 1001142970, 1001125540, 1001032690, || 1001002040, 1000924790, 1000908060, 1000756340 || 1000750730, 1000714710. B30 1002517610.
  • Manufacturer
  • 1 Event

Fabricante

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NIDFSINVIMA

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    Catalog Number: 537300-537308 Batch Number: viz příloha ( součást FSN)
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    Diagnostic medical devices in vitro
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