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On the 23rd, the State Food and Drug Administration issued an announcement that many companies and companies have voluntarily recalled their related illegal medical device products, including revision femoral stems and nylon sutures
EUROSILICONE SAS voluntarily recalls Mammary Implantable Paragel
EUROSILICONE SAS voluntarily recalls Mammary Implantable ParagelWuxi Like Trading Co.
Attachment: Medical Device Recall Event Report Form
Biomet Orthopedics voluntarily recalled Arcos Modular Revision System for revision femoral stems and accessories
Biomet Orthopedics voluntarily recalled Arcos Modular Revision System for revision femoral stems and accessoriesZimmer (Shanghai) Medical International Trade Co.
Attachment: Medical Device Recall Event Report Form
Mani, Inc.
Mani, Inc.
Attachment: Medical Device Recall Event Report Form
Mani Co.
Mani Co.
Attachment: Medical Device Recall Event Report Form
Mani Co.
Mani Co.