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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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12 records meeting your search criteria returned- Product Code: BSZ Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA FABIUS TIRO 08/10/2021
DRÄGERWERK AG & CO. KGAA APOLLO 07/29/2021
TRI-ANIM OHMEDA 03/04/2019
TRI-ANIM OHMEDA 03/04/2019
TRI-ANIM OHMEDA 03/04/2019
DRAEGERWERK AG & CO. KGAA PERSEUS A500 01/25/2019
DRÄGERWERK AG & CO. KGAA PRIMUS 12/20/2018
DRÄGERWERK AG & CO. KGAA PERSEUS A500 10/15/2018
DRÄGERWERK AG & CO. KGAA PRIMUS 09/19/2018
GE HEALTCARE AISYS 01/30/2018
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