8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PDI STERILE LUBRICATING JELLY
FDA 510(k)
FDA Class 1
·General Hospital
KODATROL I AND II CONTROL AND DILUENT SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
FUKUDA DENSHI MODEL FCP-231
FDA 510(k)
FDA Class 2
·Cardiovascular
PROFILE BIABUT 4.0 -Ø5.5
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 24, 2026
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 22, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code NBW·January 31, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 4, 2014
IRC2100 W/ 210 LIGHTGUIDE
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code KNS·August 28, 2019