50 results
·
46ms
·
Sources: EU EUDAMED, US FDA
Medicore Co., Ltd
Device
EU MDR
·
Eu Md Class 2a
·Medicore Co., Ltd·On the market·3 countries
Medicore Co., Ltd
Device
EU MDR
·
Eu Md Class 2a
·Medicore Co., Ltd·On the market·3 countries
Medicore Co., Ltd
Manufacturer
🇰🇷 South Korea·2 Basic UDI-DIs·2 Devices
IRIS-XP
FDA UDI
Medicore Co., Ltd.·00191237000069·
Max Pulse
FDA UDI
Medicore Co., Ltd.·00191237000038·
SA-3000P
FDA UDI
Medicore Co., Ltd.·00191237000014·
MEDICORE CO. LTD.
FDA registration
MEDICORE CO. LTD.·2 products·🇰🇷 South Korea
MEDICORE CO., LTD.
FDA registration
MEDICORE CO., LTD.·1 product·🇰🇷 South Korea
GFX 460
FDA Adverse Event
Injury
·MEDICORE CO. LTD.·Product code FTR·May 21, 2021
Max Pulse
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Medicore Co., Ltd·1 device
SA-3000P
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Medicore Co., Ltd·1 device
MedSystem s.r.o.
Authorized representative
🇨🇿 Czechia·1 Manufacturer·2 Devices
PRESTIGE MEDICARE Co., Ltd.
Manufacturer
🇰🇷 South Korea
Seoulin Medicare Co., Ltd.
Manufacturer
🇰🇷 South Korea·1 Importer
BK MEDICARE CO., LTD.
FDA registration
BK MEDICARE CO., LTD.·4 products·🇰🇷 South Korea
Sungshim Medicare Co.,Ltd.
FDA registration
Sungshim Medicare Co.,Ltd.·3 products·🇰🇷 South Korea
XIANTAO MEDICARE PROTECTIVE PRODUCTS CO.,LTD.
Manufacturer
🇨🇳 China
Suqian Medicom Medical Products Co., Ltd.
Manufacturer
🇨🇳 China·1 Importer
Wuxi Medicare Sanitary Products Co.,Ltd.
Manufacturer
🇨🇳 China
HENRY SCHEIN
FDA Adverse Event
Malfunction
·A.R. MEDICOM INC. (SHANGHAI) CO.,LTD.·Product code EFN·February 2, 2018