114 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIFESIGN DOA 4 (THC/OPI/COC/MET)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BBIG
FDA UDI
BBig B.V.·08719616000039·0014193
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570753·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570746·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570708·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570760·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570722·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033570739·
HEMOCHRON KAOLIN-ACTIVATED HEPARIN AND PROTAMINE DOSING ASSAYS
FDA 510(k)
FDA Class 2
·Hematology
NAC PLUS NEEDLELESS ACCESS CONNECTOR
FDA 510(k)
FDA Class 2
·General Hospital
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE AG·Product code LZG·March 21, 2013
ATTAIN OTW
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 22, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026