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Crédits
Devices
Device Recall Portex Polar Preformed Tracheal Tube
Modèle / numéro de série
Product manufactured before September 2009 and within its expiration date.
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution -- United States, Andorra, Argentina, Armenia, Australia, Austria, Bahrain, Bangladesh, Barbados, Belgium, Bermuda, Borneo, Brazil, Brunei, Bulgaria, Canada, Chile, China, C¿¿te d'Ivoire, Czech Republic, Denmark, East Timor, Egypt, Estonia, Finland, France, Georgia, Germany, Gibraltar, Greece, Guatemala, Vatican City, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Kuwait, Lebanon, Libya, Liechtenstein, Lithuania, Luxembourg, Malaysia, Maldives, Malta, Mexico, New Zealand, Netherlands, Norway, Oman, Pakistan, Panama, Philippines, Poland, Portugal, Qatar, Romania, Russian Federation, Saudi Arabia, Senegal, Singapore, Slovakia, South Africa, South Korea, Spain, Sri Lanka, Suriname, Sweden, Switzerland, Syria, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, United Kingdom and Uruguay.
Description du dispositif
Portex¿ Polar Preformed Tracheal Tube, South Oral, Murphy Eye, Clear 3.5 mm || Product Code: 100/134/035. || Intended for oral and/or nasal intubation for airway management.
Manufacturer
Smiths Medical
2 Events
Rappel de Device Recall Portex Polar Preformed Tracheal Tube
Rappel de Device Recall Portex Polar Preformed Tracheal Tube
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Fabricant
Smiths Medical
Adresse du fabricant
Smiths Medical, Hythe, Hythe, Kent United Kingdom
Société-mère du fabricant (2017)
Smiths Group Plc
Source
USFDA
Language
English
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