DRG
2026-01-22
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
QIH
2026-01-22
AI-Rad Companion Brain MR
查看詳情 →
KGN
2026-01-22
Device 104 Particulate
查看詳情 →
SHB
2026-01-21
Nova Max Creat eGFR Monitoring System
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DQX
2026-01-21
InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)
查看詳情 →
IYE
2026-01-21
Halcyon, Ethos Radiotherapy System (5.0)
查看詳情 →
QEW
2026-01-21
RoVo Mechanical Thrombectomy System
查看詳情 →
HRS
2026-01-21
Arthrex Variable Angle (VA) Proximal Tibia Plating System
查看詳情 →
EBF
2026-01-21
LumiCera
查看詳情 →
QFX
2026-01-21
Affirm 400
查看詳情 →
NKG
2026-01-21
Infinity™ OCT System
查看詳情 →
GEX
2026-01-21
Boston Pico755
查看詳情 →沒有符合的裝置。
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