10,000 results
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100ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEK
FDA 510(k)
FDA Class 1
·Hematology
HEK
FDA 510(k)
FDA Class 1
·Hematology
HEK GENCELLS
FDA 510(k)
FDA Class 1
·Hematology
S5 SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTQ·June 4, 2025
SOLIDLOK HEK TIP 3.5MM
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC.·Product code LXH·November 28, 2007
S5 ROLLER PUMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTQ·July 31, 2024
S5 MAST ROLLER PUMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTQ·December 19, 2023
S5 SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTQ·March 20, 2018
NICOLET ELITE WATERPOOF 2MHZ DOPPLER PROBE
FDA Adverse Event
Other
·NICOLET VASCULAR·Product code HEK·January 31, 2002
TALENT TAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 15, 2015
UNK - MONO/POLY SCREWS: SYNAPSE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code NKB·May 13, 2021
SYNVISC
FDA Adverse Event
Injury
·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·November 5, 2013
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·LIVANOVA USA, INC.·Product code LYJ·January 19, 2017
Expression Systems
FDA UDI
Expression Systems, LLC·00850047921413·
Monitor, Heart Sound, Fetal, Ultrasonic
FDA classification
FDA Class 2
·Monitor, Heart Sound, Fetal, Ultrasonic
ITL Dental
FDA UDI
EMERY ENTERPRISES INC·00817686024417·BEK Bone Expander Kit
CHEK MEDICAL
FDA registration
CHEK MEDICAL·2 products·🇺🇸 United States
LERADO H.K. LTD.
FDA registration
LERADO H.K. LTD.·15 products·🇨🇳 China
ITLDental
FDA UDI
EMERY ENTERPRISES INC·00817686029016·Bone Expander Kit With 5 Expanders
N/A
FDA UDI
CAREFUSION 2200, INC·10885403423987·Economy Bone Marrow Biopsy Tray, Without Biopsy...