58 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Bashan TDP Heat Lamp
FDA 510(k)
FDA Class 2
·Physical Medicine
Catalano Lacrimal Intubation Set
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896116955·Catalano Lacrimal Intubation Set 2 Blunt Probe ...
BI-METRIC HEAD/NECK HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304223141·
FLEBOSET DOUBLE
FDA 510(k)
FDA Class 2
·General Hospital
NUVASIVE ACP4 SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
STERILMED, INC.·10888551007405·SAW BLADE SAGITTAL K6 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007474·SAW BLADE SAGITTAL K6 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007436·SAW BLADE SAGITTAL K6 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007450·SAW BLADE SAGITTAL K6 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007481·SAW BLADE SAGITTAL K6 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007467·SAW BLADE SAGITTAL K6 K2000 SERIES
V.A.C.ULTA THERAPY SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·July 23, 2021
CAPSUREFIX MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code NVN·October 10, 2014
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 14, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·June 11, 2013
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020
GLIDEWIRE ADVANTAGE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022
VANGUARD CR LIP TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 14, 2017
CAPIOX RX OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 28, 2019