10,000 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
Fehling Instruments GmbH & Co. KG·04058749058338·CERAMO GRUENWALD rongeur, 30° angled up, 2.0 x ...
NEUROMARK® Device
FDA UDI
NEURENT MEDICAL LIMITED·05391537940095·The NEUROMARK System is intended for the applic...
QUICKIE Q2
FDA Adverse Event
Malfunction
·SUNRISE MEDICAL (US) LLC·Product code IOR·August 5, 2021
ASCENT REPROCESSED TROCAR B5LT
FDA Adverse Event
Malfunction
·ASCENT HEALTHCARE SOLUTIONS·Product code NMK·February 26, 2010
EDWARDS PASCAL PRECISION
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NMK·October 27, 2025
BRK
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code NMK·August 12, 2023
BRK
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code NMK·August 12, 2023
REPROCESSED ETHICON TROCAR
FDA Adverse Event
Malfunction
·ASCENT HEALTHCARE SOLUTIONS·Product code NMK·February 7, 2008
Trocar, Reprocessed
FDA classification
FDA Class 2
·Trocar, Reprocessed
NMS TECHNOLOGIES
FDA registration
NMS TECHNOLOGIES·4 products·🇨🇳 China
NML Medical, LLC
FDA registration
NML Medical, LLC·17 products·🇺🇸 United States
N.K RUBBER (M) SDN. BHD.
FDA registration
N.K RUBBER (M) SDN. BHD.·1 product·🇲🇾 Malaysia
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295074304·AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARI...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295074748·AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARI...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295039617·AMK TOTAL KNEE SYSTEM ALL POLY PATELLA COOKIE C...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295073994·THE AMK TOTAL KNEE SYSTEM PRIMARY LOCKING PIN
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295067054·AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARI...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295067221·AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARI...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295067245·AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARI...
AMK
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295039594·AMK TOTAL KNEE SYSTEM ALL POLY PATELLA COOKIE C...