Covidien LLC

17 dispositifs dans la base de données

  • Modèle / numéro de série
    Catalog Number: 64082
  • Description du dispositif
    Medical devices for single use
  • Modèle / numéro de série
    Catalog Number: 980X3DEDRAC, 980X1DEDRAC, 980X3NLDRAC, 980X1NLDRAC, 980X1FRAIQC, 980X3FRAIQC, 980X1BGDRAC, 980X1ENDRAC, 980X3CSNISC, 980X2FRAIQC, 980X3ENDRAC, 980X2DEDRAC, 980X1ELAIQC, 980X3HUNISC, 980X1ITDIEC 980X3ITDIEC, 980X1HUNISC, 980X1ENNISB 980X3ENNISB, 980X2ITDIEC, 980X1NOAIQC 980X1FIAIQC, 980X1SVAIQC, 980X3PLDIPC 980X1PLDIPC, 980X2PLDIPC, 980X1PTDIPC 980X3PTDIPC, 980X3RODRAC, 980X1RODRAC 980X3SKNISC, 980X1SKNISC, 980X1SLDRAC 980X3ESDIEC, 980X1ESDIEC, 980X2ESDIEC 980X3SVAIQC, 980X1DEDISS, 980X1FRDISS 980X3DEDISS, 980X3TRDRAC, 980X1TRDRAC Batch Number: PB980 Li-ion Battery: Serial Number range: 1201xxxxxx through 1712xxxxxx.
  • Description du dispositif
    Anesthetic and respiratory medical devices
  • Modèle / numéro de série
    Catalog Number: GPS36
  • Description du dispositif
    Medical devices for single use
  • Modèle / numéro de série
    Catalog Number: EGIARADXT Batch Number: N6L0351X
  • Description du dispositif
    Medical devices for single use
  • Modèle / numéro de série
    Catalog Number: CA15L1, CA20L1, CA30L1, CA15L2, CA20L2 & CA30L2 Batch Number: All
  • Description du dispositif
    Medical devices for single use
12 en plus

62 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    TDMDAT
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    TDMDAT
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NIDFSINVIMA
57 en plus