35 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BD PowerPiCC Catheter
FDA 510(k)
FDA Class 2
·General Hospital
300XL
FDA UDI
Smith & Nephew, Inc.·00885554011067·KIT 300XL HERMES UK
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777518·LUMBAMED PLUS FLEX PAD M SILVER IV
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777464·LUMBAMED PLUS FLEX PAD WM SILVER IV
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319744826·Lambotte Osteotome 6-3/4" (16.9cm), 8mm wide, c...
Radius Plate PROlock, Wide
FDA UDI
I.T.S. GmbH·09120034303203·Radius Plate PROlock, Wide, 4-Hole, Left
KONAN SPECULAR MICROSCOPE XIV
FDA 510(k)
FDA Class 2
·Ophthalmic
NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX
FDA 510(k)
FDA Class 2
·Anesthesiology
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·May 27, 2016
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·October 22, 2008
MULTIDIAGNOST ELEVA
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code KPR·August 8, 2011
ENDOTAK C
FDA Adverse Event
Malfunction
·HISTORICAL CPI ST. PAUL·Product code NVY·July 8, 2013
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·May 22, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·December 19, 2023
SQUARE SCREWDRIVER
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·November 26, 2019
CARTO 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·June 14, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024
CARTO 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·November 27, 2023
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·December 26, 2023