10,000 results
·
16ms
·
Sources: EU EUDAMED, US FDA
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·June 3, 2014
ALARIS® PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·February 27, 2017
DRIGARD TOWELS
FDA Adverse Event
Injury
·CROSSTEX INTERNATIONAL INC.·Product code KHR·March 26, 2019
DRY TIPS
FDA Adverse Event
Injury
·YOUNG MICROBRUSH LLC·Product code KHR·September 16, 2016
Absorber, Saliva, Paper
FDA classification
FDA Class 1
·Absorber, Saliva, Paper
Kehr Surgical Private Limited
Manufacturer
🇮🇳 India·1 Importer
Persona C HR
FDA 510(k)
FDA Class 2
·Radiology
AHRS EPILATOR 629
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
TOTAL ith. ihr. ltd. sti.
Manufacturer
🇹🇷 Türkiye
Vrták 3HR-2,0
Device
EU MDR
·
Eu Md Class 1
·MARTIKAN s.r.o.·On the market·2 countries
Vrták 3HR-1,5
Device
EU MDR
·
Eu Md Class 1
·MARTIKAN s.r.o.·On the market·2 countries
Vrták 3HR-1,3
Device
EU MDR
·
Eu Md Class 1
·MARTIKAN s.r.o.·On the market·2 countries
Vrták 3HR-1,0
Device
EU MDR
·
Eu Md Class 1
·MARTIKAN s.r.o.·On the market·2 countries
Drive
FDA UDI
Drive Devilbiss Healthcare·00822383212296·Bariatric Bed Pkg, 1pkg/cs
Drive
FDA UDI
Drive Devilbiss Healthcare·00822383212333·BariatricBed,FullElectric,48",1/cs
ANHUI CHR SOFTWARE TECHNOLOGY LIMITED COMPANY
FDA registration
ANHUI CHR SOFTWARE TECHNOLOGY LIMITED COMPANY·11 products·🇨🇳 China
Medi-Test Glucose BHR
Device
EU IVDR
·
Eu Ivd Class B
·MACHEREY-NAGEL GmbH & Co. KG·Not intended for eu market
AHR-3000 RE-USE ADAPTOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BHR BIPOLAR FEMORAL HEAD COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Biolot Medikal Malzemeleri Arge İth. İhr. Aş.
Manufacturer
🇹🇷 Türkiye·1 Basic UDI-DI·1 Device