Synchro 2 Guidewire

  • Model / Serial
    Model: SYNCHRO 2/14 200 CM STANDARD, SYNCHRO 2/14 200 CM SOFT, SYNCHRO 2/14 300 CM STANDARD, SYNCHRO 2/14 300 CM STANDARD, Affected:
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    NZMMDSA

7 devices with a similar name

Learn more about the data here

  • Model / Serial
    Material Number M00326010 Lot/Best By date: B18002 10/31/2011 B18810 1/31/2012 B18112 10/31/2011  B18113 10/31/2011  B18114 10/31/2011  B18192 11/30/2011  B18193 11/30/2011  B18194 11/30/2011  B18195 11/30/2011  B18255 11/30/2011  B18256 11/30/2011  B18257 11/30/2011  B18258 11/30/2011  B18262 11/30/2011  B18263 11/30/2011  B18264 11/30/2011  B18265 11/30/2011  B18314 11/30/2011  B18434 12/31/2011  B18435 12/31/2011  B18436 12/31/2011  B18437 12/31/2011  B18438 12/31/2011  B18439 12/31/2011  B18471 12/31/2011  B18472 12/31/2011  B18473 12/31/2011  B18474 12/31/2011  B18475 12/31/2011  B18476 12/31/2011  B18477 12/31/2011  B18531 12/31/2011  B18532 12/31/2011  B18533 12/31/2011  B18700 12/31/2011  B18737 1/31/2012  B18738 1/31/2012  B18739 1/31/2012  B18775 1/31/2012  B18776 1/31/2012  B18806 1/31/2012  B18807 1/31/2012  B18808 1/31/2012  B18809 1/31/2012  B18810 1/31/2012 B18837 1/31/2012  B18838 1/31/2012  B18839 1/31/2012  B18840 1/31/2012  B18933 1/31/2012  B18985 3/31/2012  B18986 2/29/2012  B19052 2/29/2012  B19053 2/29/2012  B19119 2/29/2012  B19181 3/31/2012  B19186 3/31/2012  B19343 3/31/2012  B19344 3/31/2012  B17178 7/31/2011  B17179 7/31/2011  B17180 7/31/2011  B17181 7/31/2011  B17182 7/31/2011  B17183 7/31/2011  B17321 8/31/2011  B17322 8/31/2011  B17323 8/31/2011  B17324 8/31/2011  B17325 8/31/2011  B17326 8/31/2011 B17386 8/31/2011 B17387 8/31/2011 B17388 8/31 2011 B17389 8/31/2011  B17438 8/31/2011  B17439 8/31/2011  B17466 8/31/2011  B17467 8/31/2011  B17468 8/31/2011  B17505 8/31/2011  B17506 8/31/2011  B17599 9/30/2011  B17600 9/30/2011  B17601 9/30/2011  B17657 9/30/2011  B17658 9/30/2011  B17659 9/30/2011  B17660 9/30/2011  B17661 9/30/2011  B17662 9/30/2011  B`7663 9/30/2011  B17707 9/30/2011  B17708 9/30/2011  B17709 9/30/2011  B17710 9/30/2011  B17711 9/30/2011  B17712 9/30/2011  B17713 9/30/2011  B17820 10/31/2011  B17821 10/31/2011  B17822 10/31/2011  B17823 10/31/2011  B17824 10/31/2011  B17912 9/30/2011  B17923 10/31/2011  B17924 10/31/2011  B17925 10/31/2011  B17926 10/31/2011  B17927 10/31/2011  B17928 10/31/2011  B17929 10/31/2011  B17978 10/31/2011  B17979 10/31/2011  B17980 10/31/2011  B17981 10/31/2011  B17982 10/31/2011  B17983 10/31/2011  B18000 10/31/2011  B18001 10/31/2011  B17203 7/31/2011  B17204 7/31/2011  B17205 7/31/2011  B17206 7/31/2011  B17207 7/31/2011  B17276 7/31/2011  B17277 7/31/2011  B17278 7/31/2011  B17279 7/31/2011  B17280 7/31/2011  B17516 8/31/2011  B17517 8/31/2011  B17518 8/31/2011  B17519 8/31/2011  B17520 8/31/2011  B17588 8/31/2011  B17589 8/31/2011  B17590 8/31/2011  B17591 8/31/2011  B17592 9/30/2011  B17593 9/30/2011  B17812 9/30/2011  B17813 9/30/2011  B17814 9/30/2011  B17815 9/30/2011  B17816 9/30/2011  B17862 9/30/2011  B17863 9/30/2011  B17864 9/30/2011  B17865 9/30/2011  B17866 9/30/2011  B17867 9/30/2011  B18011 10/31/2011  B18012 10/31/2011  B18013 10/31/2011  B18014 10/31/2011  B18015 10/31/2011  B18016 10/31/2011  B18101 10/31/2011  B18102 10/31/2011  B18103 10/31/2011  B18104 10/31/2011  B18105 10/31/2011  B18330 11/30/2011
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including CA, CO, IN, MD, MI, OR, TX, and VA and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Great Britian, Greece, Honduras, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Puerto Rico, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Switzerland, Thailand, Tunisia, Turkey, and Ukraine.
  • Product Description
    Boston Scientific brand Synchro 2 Guidewire, 0.14" 200 cm Soft. || Boston Scientific; Made in: 2405 West Orton Circle, West Valley City, UT 84119 || The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures. || Product is distributed by Boston Scientific Corporation, || Fremont, CA
  • Manufacturer
  • Model / Serial
    Material # M00326110: lot/use by dates: B17094 7/31/2011  B17095 7/31/2011  B17184 7/31/2011  B17332 8/31/2011
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including CA, CO, IN, MD, MI, OR, TX, and VA and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Great Britian, Greece, Honduras, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Puerto Rico, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Switzerland, Thailand, Tunisia, Turkey, and Ukraine.
  • Product Description
    Boston Scientific brand Synchro2 0.14" Guide Wire, 200 cm, Soft Pre Shaped; || Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 || Product is distributed by Boston Scientific Corporation, || Fremont, CA || The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.
  • Manufacturer
  • Model / Serial
    Material # M00326320: lot/use by dates: B17333 8/31/2011
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including CA, CO, IN, MD, MI, OR, TX, and VA and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Great Britian, Greece, Honduras, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Puerto Rico, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Switzerland, Thailand, Tunisia, Turkey, and Ukraine.
  • Product Description
    Boston Scientific brand Synchro2 0.14" Guide Wire, 300 cm, Soft Pre Shaped; || Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 || Product is distributed by Boston Scientific Corporation, || Fremont, CA || The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.
  • Manufacturer
  • Model / Serial
    Material # M00326410: lot/use by dates: B17096 7/31/2011  B17097 7/31/2011  B17098 7/31/2011  B17099 7/31/2011  B17185 7/31/2011  B17186 7/31/2011  B17187 7/31/2011  B17188 7/31/2011  B17198 7/31/2011  B17199 7/31/2011  B17287 7/31/2011  B17288 7/31/2011  B17327 8/31/2011  B17328 8/31/2011  B17329 8/31/2011  B17330 8/31/2011  B17331 8/31/2011  B17390 8/31/2011  B17391 8/31/2011  B17392 8/31/2011  B17393 8/31/2011  B17394 8/31/2011  B17469 8/31/2011  B17470 8/31/2011  B17472 8/31/2011  B17473 8/31/2011  B17474 8/31/2011  B17504 8/31/2011  B17507 8/31/2011  B17508 8/31/2011  B17509 8/31/2011  B17510 8/31/2011  B17602 9/30/2011  B17664 9/30/2011  B17665 9/30/2011  B17714 9/30/2011  B17715 9/30/2011  B17716 9/30/2011  B17717 9/30/2011  B17718 9/30/2011  B17719 9/30/2011  B17825 10/31/2011  B17826 10/31/2011  B817851 9/30/2011  B17931 10/31/2011  B17932 10/31/2011  B17933 10/31/2011  B17934 10/31/2011  B17984 10/31/2011  B17985 10/31/2011  B17986 10/31/2011  B17987 10/31/2011  B18003 10/31/2011  B18004 10/31/2011  B18082 10/31/2011  B18198 11/30/2011  B18200 11/30/2011  B18201 11/30/2011  B18202 11/30/2011  B18259 11/30/2011 B18260 11/30/2011  B18261 11/30/2011  B18266 11/30/2011  B18267 11/30/2011  B18268 11/30/2011  B18315 11/30/2011  B18316 11/30/2011  B18317 11/30/2011  B18318 11/30/2011  B18319 11/30/2011  B18394 12/31/2011  B18444 12/31/2011  B18445 12/31/2011  B18446 12/31/2011  B18447 12/31/2011  B18448 12/31/2011  B18449 12/31/2011  B18479 12/31/2011  B18480 12/31/2011  B18481 12/31/2011  B18484 12/31/2011  B18535 12/31/2011  B18536 12/31/2011  B18537 12/31/2011  B18538 12/31/2011  B18701 12/31/2011  B18742 1/31/2012  B18743 1/31/2012  B18812 1/31/2012  B18813 1/31/2012  B18814 1/31/2012  B18815 1/31/2012  B18816 1/31/2012  B18841 1/31/2012  B18842 1/31/2012  B18934 1/31/2012  B18987 2/29/2012  B18988 2/29/2012  B19023 2/29/2012  B19024 2/29/2012  B19110 2/29/2012  B19120 2/29/2012  B19187 3/31/2012  B19346 3/31/2012  B19379 3/31/2012  819384 3/31/2012
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including CA, CO, IN, MD, MI, OR, TX, and VA and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Great Britian, Greece, Honduras, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Puerto Rico, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Switzerland, Thailand, Tunisia, Turkey, and Ukraine.
  • Product Description
    Boston Scientific brand Synchro2 0.14" Guide Wire, 200 cm, Standard; || Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 || Product is distributed by Boston Scientific Corporation, || Fremont, CA || The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.
  • Manufacturer
  • Model / Serial
    Material # M00326420: lot/use by dates: B17334 8/31/2011    B17603 9/30/2011    B17935 10/31/2011    B18203 11/30/2011    B18441 12/31/2011    B18744 1/31/2012    B18935 1/31/2012    B18945 2/29/2012    B19378 3/31/2012
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including CA, CO, IN, MD, MI, OR, TX, and VA and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Great Britian, Greece, Honduras, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Puerto Rico, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Switzerland, Thailand, Tunisia, Turkey, and Ukraine.
  • Product Description
    Boston Scientific brand Synchro2 0.14" Guide Wire, 200 cm, Standard Pre-Shaped; || Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 || Product is distributed by Boston Scientific Corporation, || Fremont, CA || The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.
  • Manufacturer
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