3,435 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GLYCEROL (GLY)
FDA UDI
RANDOX LABORATORIES LIMITED·05055273203509·
GLY-ETCH
FDA 510(k)
FDA Class 2
·Dental
GLYCEROL CONTROL (GLY CONTROL)
FDA UDI
RANDOX LABORATORIES LIMITED·05055273203516·
Glide
FDA UDI
INFINITE BIOMEDICAL TECHNOLOGIES, LLC·00850004850695·For the ErgoArm with direct grip control config...
G7
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 28, 2018
API® 20 A 25STRIPS+25MEDIA
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, SA·Product code JSP·May 24, 2021
ETHGLY200PFES
FDA UDI
UTAK LABORATORIES, INC.·B800ETHGLY200PFES0·ETHGLY200PFES
ETHGLY100PFES
FDA UDI
UTAK LABORATORIES, INC.·B800ETHGLY100PFES0·ETHGLY100PFES
GLYCOLS LEVEL 2
FDA UDI
UTAK LABORATORIES, INC.·B800UTAKSCGLY2PSD0·GLYCOLS LEVEL 2
GLYCOLS LEVEL 1
FDA UDI
UTAK LABORATORIES, INC.·B800UTAKSCGLY1PSD0·GLYCOLS LEVEL 1
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·October 20, 2018
PROFILE 8 FR. 40CC IAB WITH GLI
FDA Adverse Event
Death
·DATASCOPE CORP.·Product code KGZ·January 2, 2003
PROFILE 8 FR. 40CC IAB WITH GLI
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·April 20, 2006
PROFILE 8 FR. 40CC IAB WITH GLI
FDA Adverse Event
Injury
·DATASCOPE CORPORATION·Product code DSP·December 6, 2002
MASIMO
FDA Adverse Event
Malfunction
·MASIMO·Product code GLY·May 28, 2012
COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·April 2, 2021
COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·April 2, 2021
COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·April 2, 2021
GUIDE CATHETER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code DQY·October 2, 2021
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·August 28, 2024