2,778 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NeuroPace RNS System
SA206, SN205, SN608, SA119, ML910, SN601, SN606, SN902, ML912, ML808, ML909, ML8686, SN206, SN602
FDA registration
NINGBO BEILUN KANGYU ELECTRICAL TECHNOLOGY CO.,LTD.·1 product·🇨🇳 China
CY6115, CY6116, CY6118, CY6119, CY6120, CY6121, CY6122
FDA registration
NINGBO BEILUN KANGYU ELECTRICAL TECHNOLOGY CO.,LTD.·1 product·🇨🇳 China
DRUG STOP
FDA 510(k)
FDA Unclassified
·Unknown
COAXIAL DILATOR SET
FDA 510(k)
FDA Class 2
·Cardiovascular
SomniCheck
FDA 510(k)
FDA Class 2
·Neurology
TEARAWAY INTRODUCER SHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
HFM
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Foshan Hongfeng Co. Ltd.·1 device
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Proclaim DRG Implantable Pulse Generator
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Infinity Family of Implantable Pulse Generators
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Proclaim Family of Implantable Pulse Generators
NA
FDA UDI
WIPRO GE HEALTHCARE PRIVATE LIMITED·00840682104227·
N/A
FDA UDI
WIPRO GE HEALTHCARE PRIVATE LIMITED·00840682104210·
N/A
FDA UDI
WIPRO GE HEALTHCARE PRIVATE LIMITED·00840682104111·
N/A
FDA UDI
WIPRO GE HEALTHCARE PRIVATE LIMITED·00840682104296·
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DIVA FAMILY, SELECTION AFM C-SERIES AND T-SERIES DEVICES
shaver
FDA registration
SHENZHEN JIE BISHI TECHNOLOGY CO., LTD·1 product·🇨🇳 China
Heslpration, porcelaln
FDA registration
SKY HKMC INTERNATIONAL LIMITED·1 product·🇭🇰 Hong Kong
YINGTAN WONKA OPTICAL TECHNOLOGY CO., LTD
FDA registration
YINGTAN WONKA OPTICAL TECHNOLOGY CO., LTD·1 product·🇨🇳 China
Photon LED Light Therapy Face Mask
FDA registration
OMEDIC TECHNOLOGY (DONGGUAN) CO., LTD·1 product·🇨🇳 China