Devices

Device Recall CSECTION PK

Model / Serial
Code: 900998 Lots: 141015749 exp. 10/31/15 141015749 exp. 10/31/15 140915186 exp. 11/30/15 150116835 exp. 3/31/16 150317856 exp. 3/31/16 150317857 exp. 3/31/16 150518853 exp. 5/31/16
Product Classification
Obstetrical and Gynecological Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
C-SECTION PK 2/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate
Manufacturer
Customed, Inc
1 Event
- Recall of Device Recall CSECTION PK

Manufacturer

Customed, Inc

Manufacturer Address
Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
Manufacturer Parent Company (2017)
Customed Inc
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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