China NMPA Product Recall - Anterograde perfusion cannulation Cardioplegia Delivery Cannula

China NMPA product recall for Anterograde perfusion cannulation Cardioplegia Delivery Cannula by Medtronic Inc. published November 15, 2024. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) has published a notice regarding a Class II volu

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Record Information

Company

Medtronic Inc.

Inspection Date

Unknown Date

Product Type

ID: 003b9e90-c6b1-4b9a-af89-978fa970ea82

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