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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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171 records meeting your search criteria returned- Product Code: FPB Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
CAREFUSION ALARIS EXTENSION SET 09/18/2018
CAREFUSION ALARIS EXTENSION SET 09/18/2018
BAXTER HEALTHCARE - DOMINICAN REPUBLIC MICRO-VOLUME EXTENSION SET 06/20/2018
BAXTER HEALTHCARE - DOMINICAN REPUBLIC MICRO-VOLUME EXTENSION SET 05/21/2018
BAXTER HEALTHCARE - DOMINICAN REPUBLIC MICRO-VOLUME EXTENSION SET 03/23/2018
BAXTER HEALTHCARE - DOMINICAN REPUBLIC MICRO-VOLUME EXTENSION SET 03/23/2018
CAREFUSION ALARIS EXTENSION SET 12/19/2017
BAXTER HEALTHCARE - DOMINICAN REPUBLIC MICRO-VOLUME EXTENSION SET 12/11/2017
CAREFUSION ALARIS EXTENSION SET 08/23/2017
SMITHS MEDICAL ASD, INC. MEDEX¿ ULTRA¿ SMALL BORE EXTENSION SET 08/09/2017
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