MAX
2025-12-19
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
QJI
2025-12-19
DBLG2
查看詳情 →
KTI
2025-12-19
LIA-1 Catheter (542-1)
查看詳情 →
KTT
2025-12-19
Monkey Rings External Ring Fixation System
查看詳情 →
CAF
2025-12-19
eRapid with eTrack System
查看詳情 →
MUJ
2025-12-19
ClearCalc Model RADCA V2.6
查看詳情 →
QIH
2025-12-19
Alzevita
查看詳情 →
MBH
2025-12-19
Balanced Knee System TriMax Porous Femoral Components
查看詳情 →
NEZ
2025-12-19
CE Deliver (DLV)
查看詳情 →
OHS
2025-12-19
LED Light Therapy Device (Models: SG-FM, SG-FE)
查看詳情 →
NEU
2025-12-19
SCOUT MD Surgical Guidance System
查看詳情 →
DQK
2025-12-19
STAR Apollo™ Mapping System
查看詳情 →沒有符合的裝置。
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