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Crédits
Devices
Portex
Modèle / numéro de série
Lot numbers starting with: 1, K1, K51, K52, K53
Classification du dispositif
General Hospital and Personal Use Devices
Distribution
Nationwide
Description du dispositif
Portex Hypodermic Needle-Pro 5 ml Syringe, || 20g x 1 ¿'' Needle || Catalog Number: 4250
Manufacturer
Smiths Medical ASD, Inc.
1 Event
Rappel de Portex
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Fabricant
Smiths Medical ASD, Inc.
Adresse du fabricant
Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
Société-mère du fabricant (2017)
Smiths Group Plc
Source
USFDA
229 dispositifs médicaux avec un nom similaire
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Device Recall Portex Uncuffed Paediatric Sized 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¿ Uncuffed Paediatric Sized Tracheal Tube || Oral Nasal, Ivory 3.5 mm, || Product Code: 100/105/035. || Intended for oral and/or nasal intubation for airway management.
Manufacturer
Smiths Medical
Device Recall Portex 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¿ Tracheal Tube, Oral/Nasal, Murphy Eye, Clear, 3.5 mm || Product Code: 100/127/035. || Intended for oral and/or nasal intubation for airway management.
Manufacturer
Smiths Medical
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
Portex
Modèle / numéro de série
Lot numbers starting with: 0, 1, 909, 911, K1, K50, K51
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide
Description du dispositif
Portex ULTRA-FLO 4 ¿ Way Stopcock || Catalog Number: T1210
Manufacturer
Smiths Medical ASD, Inc.
Portex
Modèle / numéro de série
Lot numbers starting with: 0
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide
Description du dispositif
Portex High Pressure 1 - Way Stopcock || Catalog Number: T8200
Manufacturer
Smiths Medical ASD, Inc.
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