440 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749055054·CERAMO RUSKIN-LISTON bone cutting forceps, cvd....
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·June 3, 2020
NEUROVENT-P
FDA Adverse Event
Injury
·RAUMEDIC AG·Product code GWM·May 8, 2023
DRAGONFLY IMAGING CATHETER
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code NKK·June 25, 2012
QUIXIL APPLICATION DEVICE
FDA Adverse Event
Death
·OMRIX BIOPHARMACEUTICALS LTD.·Product code NKK·December 3, 2009
ULTRA FLOW
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code NKK·August 4, 2025
DRAGONFLY IMAGING CATHETER
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code NKK·August 7, 2012
DRAGONFLY IMAGING CATHETER
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code NKK·September 19, 2012
SAFETY NEEDLE
FDA Adverse Event
Malfunction
·COVIDIEN·Product code NKK·June 25, 2017
MONOJECT LIFESHIELD
FDA Adverse Event
Malfunction
·COVIDIEN LLC·Product code NKK·October 25, 2019
Needle, Hypodermic, Single Lumen, Reprocessed
FDA classification
FDA Class 2
·Needle, Hypodermic, Single Lumen, Reprocessed
KNK
FDA registration
KNK·1 product·🇰🇷 South Korea
Bebeonkers I
FDA UDI
SMALL BEGINNINGS INC·00815090011740·The Bebeonkers I Oral/Nasal Suction Device with...
Webeonkers
FDA UDI
SMALL BEGINNINGS INC·00815090011535·The Webeonkers Oral/Nasal Suction Device for th...
NUK® Double Electric Breast Pump
FDA UDI
NUK USA LLC·00885131626011·
NUK® Single Electric Breast Pump
FDA UDI
NUK USA LLC·00885131627667·
first essentials Nasal Aspirator
FDA UDI
NUK USA LLC·00885131760876·
NUK® Manual Breast Pump
FDA UDI
NUK USA LLC·00885131627735·
DKK
FDA UDI
Bioland Technology Ltd.·06939184627106·Blood glucose monitoring system, it contains bl...
N.K RUBBER (M) SDN. BHD.
FDA registration
N.K RUBBER (M) SDN. BHD.·1 product·🇲🇾 Malaysia