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Crédits
Devices
Device Recall LAPAROTOMY SURGICAL PACK
Modèle / numéro de série
Code:900281A Lots: 140814951 exp. 2/28/16 140714543 exp. 2/28/16 141015713 exp. 10/31/15 150116503 exp. 12/31/15 150116513 exp. 12/31/15 150116514 exp. 12/31/15 150116515 exp. 12/31/15 141216437 exp. 12/31/15 150116939 exp. 2/28/16 150116940 exp. 2/28/16 150116938 exp. 2/28/16 150116941 exp. 2/28/16 150116937 exp. 2/28/16 150317732 exp. 3/31/16 150317731 exp. 3/3/16 150317734 exp. 3/31/16 150317733 exp. 3/31/16 150317954 exp. 4/30/16 150317957 exp. 4/30/16 150317958 exp. 4/30/16 150317959 exp. 4/30/16 150317960 exp. 4/30/16 150317961 exp. 4/30/16 150418383 exp. 4/30/16 150418384 exp. 4/30/16 150418385 exp. 4/30/16 150518790 exp. 5/31/16 150519028 exp. 5/31/16 150519029 exp. 5/31/16
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Distributed Only in Puerto Rico.
Description du dispositif
LAPAROTOMY SURGICAL PACK 3/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
Rappel de Device Recall LAPAROTOMY SURGICAL PACK
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Fabricant
Customed, Inc
Adresse du fabricant
Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
Société-mère du fabricant (2017)
Customed Inc
Source
USFDA
Language
English
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