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

China NMPA product recall for Intra-aortic balloon counterpulsation catheter, intra-aortic balloon counterpulsation catheter and accessories by Arrow International Inc. published May 20, 2024. Recall level: Level 1 Recall. The National Medical Products Administration (NMPA) issued a significant announcement on May 20, 202

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Record Information

Company

Arrow International Inc.

Inspection Date

Unknown Date

Product Type

ID: 7a7db606-8e8b-4d50-9731-1b47bed8f5de

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