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Crédits
Manufacturers
Curlin Medical Llc
Adresse du fabricant
Curlin Medical Llc, 15751 Graham St, Huntingtn Bch CA 92649-1630
Société-mère du fabricant (2017)
Moog Inc
Source
USFDA
5 Events
Rappel de Device Recall Model 4000 Plus Ambulatory Infusion Pump
Rappel de Device Recall Model 2000 CMS/ Model 2000 Plus Ambulatory Infusion Pump
Rappel de Device Recall Model 4000 CMS Ambulatory Infusion Pump
Rappel de Device Recall Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump
Rappel de Device Recall PainSmart, PainSmart IOD Ambulatory Infusion System
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5 dispositifs dans la base de données
Device Recall Model 4000 Plus Ambulatory Infusion Pump
Modèle / numéro de série
Serial Numbers for all affected units: 100074 to 210458
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Description du dispositif
Model 4000 Plus Ambulatory Infusion Pump, Model Number: 350-1001
Device Recall Model 2000 CMS/ Model 2000 Plus Ambulatory Infusion Pump
Modèle / numéro de série
Serial Numbers for all affected units: 100074 to 210458
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Description du dispositif
Model 2000 CMS/ Model 2000 Plus Ambulatory Infusion Pump, Model Number: 340-1001
Device Recall Model 4000 CMS Ambulatory Infusion Pump
Modèle / numéro de série
Serial Numbers for all affected units: 100074 to 210458
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Description du dispositif
Model 4000 CMS Ambulatory Infusion Pump, Model Number: 350-1101
Device Recall Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump
Modèle / numéro de série
Serial Numbers for all affected units: 100074 to 210458
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Description du dispositif
Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number: 360-1101
Device Recall PainSmart, PainSmart IOD Ambulatory Infusion System
Modèle / numéro de série
Serial Numbers for all affected units: 100074 to 210458
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Description du dispositif
PainSmart, PainSmart IOD Ambulatory Infusion System, Model Number: 360-1301
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CURLIN MEDICAL LLC
Adresse du fabricant
HUNTINGTON BEACH
Société-mère du fabricant (2017)
Moog Inc
Source
HC
Curlin Medical Llc
Adresse du fabricant
Curlin Medical Llc, 15751 Graham St, Huntington Beach CA 92649-1630
Source
USFDA
Language
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