925 results
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27ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NORDENT MANUFACTURING INC
FDA UDI
NORDENT MANUFACTURING INC·00840018630680·CONDENSER - ELITE HANDLE
ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POLYESTER
FDA UDI
C.P. MEDICAL CORPORATION·10790986006536·
E-LOC ENDO 360° BARBED SUTURE
FDA UDI
ASSUT EUROPE SPA·18033439173587·
PGA
FDA UDI
C.P. MEDICAL CORPORATION·10790986006543·
PGA
FDA UDI
C.P. MEDICAL CORPORATION·10790986006550·
POLYESTER
FDA UDI
C.P. MEDICAL CORPORATION·10790986006529·
E-LOC ENDO 360° BARBED SUTURE
FDA UDI
ASSUT EUROPE SPA·18033439168897·
E-LOC NON-ABSORBABLE ENDO 360° BARBED SUTURE
FDA UDI
ASSUT EUROPE SPA·18033439171309·
Echovirus Negative Control
FDA UDI
Bion Enterprises, Ltd.·B110ECN44100·
AMA Optics Eye Chart
FDA UDI
AMA Optics, Inc.·G506VAN020·An ophthalmic retro-illuminated chart printed w...
Endophys Pressure Sensing Sheath Kit-6F
FDA UDI
ENDOPHYS HOLDINGS, LLC·00852004007017·The Endophys Pressure Sensing Sheath Kit is com...
GE CARESCAPE CENTRAL STATION
FDA Adverse Event
Malfunction
·GE·Product code MHX·September 1, 2016
ZOLL R DEFIBRILLATOR
FDA Adverse Event
Injury
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 21, 2025
ZOLL R DEFIBRILLATOR
FDA Adverse Event
Injury
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 21, 2025
ZOLL R DEFIBRILLATOR
FDA Adverse Event
Injury
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 21, 2025
PATELLA CLAMP
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·April 12, 2013
ENROUTE .014" GUIDEWIRE
FDA Adverse Event
Malfunction
·LAKE REGION MEDICAL·Product code DQX·June 16, 2025
UNIVERSAL IMPACTOR/POSTIONER
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MAY·October 13, 2015
ENROUTE .014" GUIDEWIRE
FDA Adverse Event
Malfunction
·LAKE REGION MEDICAL·Product code DQX·May 21, 2025