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Device Recall PREMIUM ARTHROSCOPY PK
Model / Serial
Code:9001298 Lots: 141015770 exp. 11/30/15 141115977 exp. 11/30/15 150116759 exp. 2/28/16
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
PREMIUM ARTHROSCOPY PK CUSTOMED 5/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 PREMIUM ARTHROSCOPY PK
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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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