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Devices
Device Recall Angiography/angioplasty kit
Model / Serial
Catalog number: 900002 Lots: 140714427 exp. 7/30/2017 141014965 exp. 7/30/2017 150116709 exp. 1/31/2016 150318103 exp. 3/31/2016 150418510 exp. 4/30/2016 150519016 exp. 5/31/2016
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
ANGIODRAPE PK 4/CS || Used by medical staff to perform surgical procedures and patient care || procedures such as wound healing, suture removals, irrigate wounds, etc.
Manufacturer
Customed, Inc
1 Event
Recall of Device Recall Angiography/angioplasty kit
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Manufacturer
Customed, Inc
Manufacturer Address
Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
Manufacturer Parent Company (2017)
Customed Inc
Source
USFDA
Language
English
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