PGM
2026-01-15
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
ODP
2026-01-15
Curiteva Porous PEEK Cervical Interbody Fusion System
查看詳情 →
QHW
2026-01-15
Bio-Medicus Life Support Catheter and Introducer
查看詳情 →
ITI
2026-01-15
Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80) (BBR-E80-02)
查看詳情 →
LBI
2026-01-15
SnugLit(TM) Wearable Phototherapy System (SNGL-01-US)
查看詳情 →
QFG
2026-01-15
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
查看詳情 →
PHX
2026-01-15
AltiVate Reverse® ADLC Glenosphere
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NRY
2026-01-15
Esperance pHLO Aspiration System
查看詳情 →
GXN
2026-01-14
METICULY Patient-specific titanium mesh implant
查看詳情 →
IYE
2026-01-14
ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface
查看詳情 →
GEI
2026-01-14
ENTire IRE System
查看詳情 →
QJI
2026-01-14
SmartGuard technology; Predictive Low Glucose technology
查看詳情 →沒有符合的裝置。
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