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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-1978-2025 - Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM001 Software Version: N/A Product Description: 1. Product Overview 1.1 Product Name: Integrated N... 2 06/13/2025 FEI # 3037392657
Guangzhou Pluslife Biotech Co., Ltd.
Z-1979-2025 - Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Catalog Number: RM1010202 Software Version: N/A Product Description: 1. Product Overview Product Name... 2 06/13/2025 FEI # 3037392657
Guangzhou Pluslife Biotech Co., Ltd.
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