74 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IMPEDIMED EXTRA CELLULAR FLUID ANALYSIS, MODEL L-DEX U400
FDA 510(k)
FDA Class 2
·Cardiovascular
X-Box
FDA UDI
INNO Holdings, Inc.·M71190808250·PEEK, Ta
CoRoent
FDA UDI
Nuvasive, Inc.·00887517283412·CoRoent® LO Ti, 8x10x25mm 5°
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014607702·STERIS-AMSCO 1080, 2080 3.25" DELUXE GEL
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197541411·RZ Tebbet Breast Retractor
80x25m...
MEDLINE STERISET STERILIZATION CONTAINER
FDA 510(k)
FDA Class 2
·General Hospital
4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
COCR FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·July 23, 2025
MASTERLOC CEMENTLESS TI COATED STD STEM SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·May 29, 2018
SPIRAL BLADE AIMING ARM FOR TI CANNULATED HUMERAL NAILS-EX
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code LXH·April 26, 2013
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 25, 2014
30327 12CC 100 UNIT HEP SYR {CAN} (5CC)
FDA Adverse Event
Malfunction
·TYCO HEALTHCARE / KENDALL·Product code NZW·July 23, 2008
LINER: MPACT FLAT PE HC 36/E
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·May 5, 2021
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019