China NMPA Product Recall - Intra-aortic balloon counterpulsation catheter and accessories; Intra-aortic balloon counterpulsation catheter

China NMPA product recall for Intra-aortic balloon counterpulsation catheter and accessories; Intra-aortic balloon counterpulsation catheter by Arrow International Inc. published April 21, 2016. Recall level: Class I Recall. Talifu Medical Devices Trading (Shanghai) Co., Ltd., acting on behalf of manufacturer Arrow Internat

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Record Information

Company

Arrow International Inc.

Inspection Date

Unknown Date

Product Type

ID: db55f970-3573-4660-876b-c615ff0e9540

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