57 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRANSTEK BLOOD PRESSURE MONITOR MODEL TMB-986, TMB-987, TMB-995
FDA 510(k)
FDA Class 2
·Cardiovascular
JOBST Bella Strong
FDA UDI
BSN MEDICAL, INC.·00035664012373·BELLA STRONG 20-30 MM HG GAUNTLET SIZE 5 NATURA...
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...
Luxe™ 2.5 Semi-custom loupe
FDA UDI
METREX RESEARCH, LLC·00850036373568·Semi-custom loupe with Luxe™ 2.5 plano oculars,...
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365119200·
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383502146·Gutta Percha Points is used to root canal filin...
BEL-CAT
FDA 510(k)
FDA Class 2
·Radiology
POSITRACE DUAL MODE PET/CT ONCOLOGY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
AS VEGA PS TIBIAL PLATEAU CEMENTED T3
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 4, 2018
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 3, 2013
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FNL·September 19, 2014
INTERSTIM
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·May 11, 2011
AS COLUMBUS REV F FEMUR CEMENTED F5L
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS VEGA PS TIBIAL PLATEAU CEMENTED T3+
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS VEGA PS TIBIAL PLATEAU CEMENTED T2
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS COLUMBUS REV F TIB.OFFSET CEMENT.T5
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 6, 2025
UNK STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·August 8, 2025
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·June 26, 2025
UNK TRILOGY SHELL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·June 24, 2025