China NMPA Product Recall - Balloon dilation catheter (model 8012020D)

China NMPA product recall for Balloon dilation catheter (model 8012020D) by Cordis Europa N.V. published July 11, 2012. Recall level: . Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. initiated a voluntary recall of its Balloon D

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Record Information

Company

Cordis Europa N.V.

Inspection Date

Unknown Date

Product Type

ID: 6dea1a74-34d6-4fc4-955f-af68a712108c

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