3,246 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Sterile wound dressing
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile wound dressing
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(GAMMA)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(GAMMA)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(ETO)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(ETO)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(ETO)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile dressing combine(ETO)
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Bowl Set
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Bowl Set
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Bowl Set
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Basic Dressing Packs
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Basic Dressing Packs
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Basic Dressing Packs
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Basic Dressing Packs
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Basic Dressing Packs
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Adhesive Wound Plasters/Strips
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Sterile Suction Catheters
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Urine bag
Device
EU MDR
·
Eu Md Class 1
·Multigate Co., Ltd·Not intended for eu market
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·INTEGRITY AFX DR MODEL 5346 DUAL CHAMBER PULSE GENERATOR AND PROGRAMMER SOFTWARE MODEL 3307, V2.2A