24 results
·
33ms
·
Sources: EU EUDAMED, US FDA
MEDICOMP, INC.
FDA registration
MEDICOMP, INC.·3 products·🇺🇸 United States
TelePatch Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000371·TelePatch CM PM700 is a small, auto triggered, ...
Epicardia 5000
FDA UDI
MEDICOMP, INC.·00862887000302·Epicardia 5000 is a screening tool for patients...
TelePatch Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000388·TelePatch CM PM750 is a small, auto triggered, ...
Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000357·Cardiac Monitor PM500 is a small, auto triggere...
Decipher Holter Monitor
FDA UDI
MEDICOMP, INC.·00862887000364·Decipher Holter Monitor is a small, patient wor...
TelePatch Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000319·TelePatch CM PM800 is a small, auto triggered, ...
CardioPAL SAVI
FDA UDI
MEDICOMP, INC.·00862887000340·CardioPAL SAVI is a small, patient worn device,...
Dujo Logos Inc. DBA: MEDICOMP MEDICAL
FDA registration
Dujo Logos Inc. DBA: MEDICOMP MEDICAL·4 products·🇺🇸 United States
TELEPATCH MONITORING SYSTEM
FDA Adverse Event
Injury
·MEDICOMP, INC.·Product code DRG·May 25, 2022
MEDI-LANCE
FDA Adverse Event
Malfunction
·MEDICORE, INC.·Product code FMK·April 4, 1996
LITE TOUCH U-100 INSULIN SYRINGE
FDA Adverse Event
MEDICORE, INC.·Product code FMF·February 14, 2000
RESP-BAC
FDA Adverse Event
MEDICOMP, INC.·Product code CAH·July 14, 1994
REACT DX
FDA Adverse Event
Injury
·MEDICOMP, INC.·Product code MLO·January 28, 2025
SUTURE ANCHOR, MICRO CORKSCREW FT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·April 29, 2024
TELEPATCH MONITORING SYSTEM
FDA Adverse Event
Injury
·REACTDX/MEDICOMP, INC.·Product code DRG·November 19, 2025
Meditrial Srl
Authorized representative
🇮🇹 Italy·2 Manufacturers·17 Devices
MEDCOMP 2.6F X 50CM DUAL LUMEN VASCU-PICC BASIC SET, PICC LINE
FDA Adverse Event
Malfunction
·MEDICAL COMPONENTS INC., (DBA MEDICOMP)·Product code LJS·December 20, 2018
1ST RESPONSE RESUSCITATOR, ADULT
FDA Adverse Event
Malfunction
·MFG BY SMITHS MED ASD, INC. BY: GALE MED CORP·Product code BTM·November 8, 2006
1ST RESPONSE RESUSCITATOR, ADULT
FDA Adverse Event
Injury
·MFG FOR SMITHS MED ASD,INC. BY GALE MED CORP.·Product code BTM·October 17, 2007