27 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Magic Torque DLVR Guidewire
FDA 510(k)
FDA Class 2
·Cardiovascular
Monoject
FDA UDI
Cardinal Health, Inc.·10884521544666·Hypodermic Safety Needle
Monoject
FDA UDI
Cardinal Health 200, LLC·10192253025057·Hypodermic Safety Needle 23G x 1.5 in.
(0.6 x 3...
AVANOS
FDA UDI
Avanos Medical, Inc.·00193493935048·AVANOS* Single-Shot Epidural Trays
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269866·
Halyard
FDA UDI
Avanos Medical, Inc.·10680651935042·HYH,EP TRY,S-SHOT,-,-,10
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304183094·
EC50 MICRO+ SMOKERLYZER
FDA 510(k)
FDA Class 2
·Anesthesiology
STAXX XDL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
I-STAT EC4+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019
I-STAT EC4+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019
I-STAT EC4+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019
I-STAT EC4+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019
I-STAT EC4+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2013
ACTIVA PC
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·July 11, 2011
CS100
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·September 30, 2008
INTERCHANGEABLE ULNAR ASSEMBLY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019
MENTOR CPX4 WITH SUTURE TABS, TALL HEIGHT, SMOOTH
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·October 24, 2019
MENTOR CPX4 WITH SUTURE TABS, MED HEIGHT, SMOOTH
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·January 10, 2020