25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EPOCH HIP PROSTHESIS, MODEL 4075 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58280140700·CURETTE
t:slim X2 Insulin Pump with Control-IQ+ Technology
FDA UDI
Tandem Diabetes Care, Inc.·00389152407012·Control-IQ 7.x
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033575901·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033575918·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558928·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558898·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558911·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558904·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0140000·Counter Torque, Standard and Extended Tab
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0140200·T-Handle, T30 Split Tip Cap Starter
R & D 4K RETIC
FDA 510(k)
FDA Class 2
·Hematology
ULTRAPAK NEHA
FDA 510(k)
FDA Unclassified
·Unknown
GOOD SAM CINCINNATI OH 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·December 11, 2008
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
TENDRIL STS
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
D-TRONPLUS POWER PACK
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·March 13, 2008
BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·October 1, 2020
BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·November 5, 2020
BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·November 5, 2020