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Device Recall UNIFUSE INFUSION SYSTEM
Model / Serial
Lot 521388 (Use By 2013-07)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA and The Netherlands.
Product Description
ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF 12401818, CATHETER SIZE 4F, CATHETER LENGTH 90 cm, INFUSION LENGTH 10 cm, OCCLUSION WIRE SIZE .035 in., STERILE, AngioDynamics Inc., 603 Queensbury Avenue, Queensbury, NY 12804
Manufacturer
Angiodynamics Worldwide Headquarters
1 Event
Recall of Device Recall UNIFUSE INFUSION SYSTEM
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Manufacturer
Angiodynamics Worldwide Headquarters
Manufacturer Address
Angiodynamics Worldwide Headquarters, 14 Plaza Drive, Latham NY 12110-3421
Manufacturer Parent Company (2017)
AngioDynamics Inc
Source
USFDA
One device with a similar name
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Device Recall UNIFUSE INFUSION SYSTEM
Model / Serial
Lot 521372 (Use By 2013-07)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA and The Netherlands.
Product Description
ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF 12401819, CATHETER SIZE 4F, CATHETER LENGTH 90 cm, INFUSION LENGTH 20 cm, OCCLUSION WIRE SIZE .035 in., STERILE, AngioDynamics Inc., 603 Queensbury Avenue, Queensbury, NY 12804
Manufacturer
Angiodynamics Worldwide Headquarters
Language
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