LRX
2026-02-10
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
KDI
2026-02-10
multiFlux 130 (F00013123); multiFlux 160 (F00013124)
查看詳情 →
KGN
2026-02-10
CollOvine™ Wound Powder
查看詳情 →
NKB
2026-02-10
Vulcan Spinal System
查看詳情 →
MOS
2026-02-10
GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive Only
查看詳情 →
MJV
2026-02-10
Earflo (EF001)
查看詳情 →
OVB
2026-02-10
SpaceOAR Vue System (SV-2101)
查看詳情 →
NHA
2026-02-10
Solidex® Ti-Links and Screws
查看詳情 →
ETN
2026-02-10
NIM Essence™ EMG Endotracheal Tube (NIMEID060); NIM Essence™ EMG Endotracheal Tube (NIMEID065); NIM Essence™ EMG Endotracheal Tube (NIMEID070); NIM Essence™ EMG Endotracheal Tube (NIMEID075); NIM Essence™ EMG Endotracheal Tube (NIMEID080)
查看詳情 →
QIH
2026-02-10
MI View&GO
查看詳情 →
DQK
2026-02-09
Holter ECG and ABP system (HolterABP)
查看詳情 →
DYB
2026-02-09
Peel-Away Introducer Sheath
查看詳情 →沒有符合的裝置。
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