4,947 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NaviCam Tether
FDA UDI
ANX ROBOTICA CORP·00850015518287·Tether Accessory. The NaviCam Capsule and NaviC...
36M - Cee-Us - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588210001·36M - Cee-Us - Metal
24M - Cee-Us - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588180601·24M - Cee-Us - Metal
Cee-Us - 18 Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588210032·Cee-Us - 18 Metal
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094264272·H3+ 3-channel digital Holter Recorder - 7-day, ...
HSB - Personal Protection - 36 Cee-Us
FDA UDI
Certified Safety Manufacturing, Inc.·00766588180052·HSB - Personal Protection - 36 Cee-Us
CEEON
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, GRONINGEN·Product code HQL·December 23, 2002
VitalFlow Power Cord CEE 7/7, 2.5m
FDA UDI
MICHIGAN CRITICAL CARE CONSULTANTS, INC.·10850007732292·AC Power Cord (EU Type F, CEE 7/7, 2.5m) for Vi...
CREATININE PLUS VER.2
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JFY·February 28, 2025
ELIX
FDA Adverse Event
Malfunction
·EMD MILLIPORE CORPORATION·Product code FIP·May 12, 2015
CARDIOSAVE HYBRID W/ E/F PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·April 3, 2025
CEE-ON LENS
FDA Adverse Event
Injury
·PHARMACIA PRODUCTION B.V.·Product code HQL·April 25, 1997
CEE ON LENS
FDA Adverse Event
Injury
·PHARMACIA BV PRODUCTION·Product code HQL·August 18, 1999
CEE ON LENSES
FDA Adverse Event
Malfunction
·PHARMACIA IOVISION, INC.·Product code HQL·March 6, 1998
CEE ON LENS
FDA Adverse Event
Injury
·PHARMACIA BV PRODUCTION·Product code HQL·March 27, 1998
CEE ON LENS
FDA Adverse Event
Injury
·PHARMACIA IOVISION, INC.·Product code HQL·March 27, 1998
EXERCISER
FDA Adverse Event
Malfunction
·BIODYNAMIC TECHNOLOGIES OF FLORIDA·Product code BXB·March 24, 1994
CARDIOSAVE HYBRID W/ E/F PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·November 19, 2025
CEEON LENS
FDA Adverse Event
Injury
·PHARMACIA BV PRODUCTION·Product code HQL·September 8, 1999
PREMIUM PLUS CEE 28
FDA Adverse Event
Malfunction
·COVIDIEN UNITED STATES SURGICAL CORPORATION·Product code GDW·November 9, 2009