26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APPLIED GELPORT LAPAROSCOPIC HAND ACCESS DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450743317·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0140070·T-Handle, T30, Locking Cap Adjuster
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556337·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556382·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0140400·Driver Shaft, T30 Final Cap Driver
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556443·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556436·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556429·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556412·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033556399·
INSTANT-VIEW PHENCYCLIDINE (PCP) URINE CASSETTE TEST
FDA 510(k)
FDA Unclassified
·Unknown
HOME-AWAY SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
HEARTSINE SAMARITAN 300P AND PAD-PAK K014067
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·July 19, 2018
HEARTSINE SAMARITAN 300P AND PAD-PAK K014067
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·March 7, 2018
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
INTEGRITY AFX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2011
UV-FLASH SOLUTION TRANSFER SET (SHORT) - JAPAN
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 14, 2008
M2A-MAGNUM PF CUP 48ODX42ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 11, 2014
M2A-MAGNUM MOD HD SZ 42MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 11, 2014