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Crédits
Devices
Device Recall Super ArrowFlex Percutaneous Sheath Introducers
Modèle / numéro de série
All lots of Product codes listed in Z-1489-2009.
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide distribution: USA, Argentina, Australia, Bahamas, Belarus, Belgium, Brazil, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Finland, France, Germany, Greece, Guatemala, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Latvia, Lithuania, Malaysia, Mexico, Netherlands, New Zealand, Norway, Pakistan, Peru, Philippines, Poland, Singapore, Slovakia, South Africa, South Korea, Spain, Sri lanka, Sweden, Taiwan, Thailand, Tunisia, Turkey, UK, Ukraine, and Venezuela.
Description du dispositif
Arrow Super Arrow-Flex Percutaneous Sheath Introducers
Manufacturer
Arrow International Inc
1 Event
Rappel de Device Recall Super ArrowFlex Percutaneous Sheath Introducers
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Fabricant
Arrow International Inc
Adresse du fabricant
Arrow International Inc, 2400 Bernville Road, Reading PA 19605
Société-mère du fabricant (2017)
Teleflex Incorporated
Source
USFDA
Language
English
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