15 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SYNTHES ZERO-P
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Scissors
FDA UDI
Medetz Surgical Instruments LLC·G2231124590·Stevens tenotomy scissors straight blades with ...
MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
NEXSTAT (TM) TOPICAL HEMOSTAT POWDER; NEXFOAM (R) TOPICAL SPONGE
FDA 510(k)
FDA Unclassified
·Unknown
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973257·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973301·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970041·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970065·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973837·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970058·
ASAHI CONFIANZA PTCA GUIDE WIRE
FDA Adverse Event
Malfunction
·AV-ASAHI·Product code DQX·May 14, 2013
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 24, 2014
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·April 28, 2011
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021
Model Number L131, ESSENTIO DR EL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025