China NMPA Product Recall - Semi-automatic external defibrillator
China NMPA product recall for Semi-automatic external defibrillator by Philips Medical Systems published March 17, 2021. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) announced on March 17, 2021, a voluntary Class I
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China NMPA product recall for Semi-automatic external defibrillator by Philips Medical Systems published March 17, 2021. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) announced on March 17, 2021, a voluntary Class I
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Company
Philips Medical SystemsInspection Date
Unknown Date
Product Type
ID: 09930195-f370-4dc4-8f66-2b8449003c88
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