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Crédits
Manufacturers
Terumo Medical Corp
Adresse du fabricant
Terumo Medical Corp, 2101 Cottontail Ln, Somerset NJ 08873-1277
Société-mère du fabricant (2017)
Terumo Corp.
Source
USFDA
19 Events
Rappel de AngioSeal Evolution
Rappel de Terumo Medical Corporation
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Rappel de Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
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19 dispositifs dans la base de données
AngioSeal Evolution
Modèle / numéro de série
5980075, 5980077
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
No
Distribution
Distributed to accounts in AL, CA, FL, IA, IN, MI, MO, NC, NY, SD, TN, and TX.
Description du dispositif
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Terumo Medical Corporation
Modèle / numéro de série
150401 150429 150713 150821 150923 151009 160314 150413 150501 150708 150824 150915 151013 151111 150415 150515 150701 150716 150902 151005 151106 150407 150514 150707 150827 151008 151109 160509 150406 150501 150713 150716 150825 151001 151102 160315 160509 150410 150710 150831 150909 151007 151012 151014 151103 151208 150417 150429 150717 150910 151002 151102 160510 150408 150429 150701 150717 150831 151013 151103 160512 150409 150430 150518 150703 150706 150903 150914 151005 150331 150430 150708 150714 150904 150910 151001 151102 150414 150429 150715 150903 151005 151029 160323 150416 150518 150715 150908 150915 151002 151106 160328 150401 150430 150716 150828 151006 150403 150514 150717 150901 150909 151012 150408 150430 150713 150907 151001 150402 150512 150713 150907 151001
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Nationwide
Description du dispositif
MISAGO RX Self Expanding Peripheral Stem
Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Modèle / numéro de série
Lot s 161019, 161108, 161215, 170112, 170213, 170314
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada
Description du dispositif
Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 16CM (0.021), REF/Product Code RM*RS7F16PA, STERILE, Rx ONLY
Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Modèle / numéro de série
Lot s 161109, 161216, 170118, 170126
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada
Description du dispositif
Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021), REF/Product Code RM*RS7F10PA, STERILE, Rx ONLY
Device Recall Glidesheath Slender Hydrophilic Coated Introducer Sheath
Modèle / numéro de série
Lot s 161115, 161130, 161207, 170116
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada
Description du dispositif
Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 10CM (0.025), REF/Product Code RM*RS6J10PA, STERILE, Rx ONLY
14 en plus
19 fabricants avec un nom similaire
En savoir plus sur les données
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Terumo Corporation || Terumo Medical Corporation
Société-mère du fabricant (2017)
Terumo Corp.
Source
NIDFSINVIMA
TERUMO MEDICAL CORPORATION (ELKTON)
Société-mère du fabricant (2017)
Terumo Corp.
Source
MSHM
TERUMO MEDICAL CORPORATION
Société-mère du fabricant (2017)
Terumo Corp.
Source
MSHM
Terumo Medical Corp
Adresse du fabricant
Terumo Medical Corp, 2101 Cottontail Lane, Somerset NJ 08873-1277
Société-mère du fabricant (2017)
Terumo Corp.
Source
USFDA
Terumo Medical Corporation
Adresse du fabricant
Terumo Medical Corporation, 950 Elkton Blvd, Elkton MD 21921-5322
Société-mère du fabricant (2017)
Terumo Corp.
Source
USFDA
14 en plus
Language
English
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