GWM
2026-04-10
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
SHQ
2026-04-10
TRIOS Dx (R1)
查看詳情 →
LRK
2026-04-10
ShaeferH
查看詳情 →
MCW
2026-04-10
Auryon Atherectomy System
查看詳情 →
KLE
2026-04-10
Porcelain Etch Gel
查看詳情 →
JKA
2026-04-10
BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection Tube
查看詳情 →
QKB
2026-04-10
AI-Rad Companion Organs RT
查看詳情 →
DYB
2026-04-10
Protaryx Transseptal Puncture Device (PTX2-001)
查看詳情 →
QIH
2026-04-10
syngo Dynamics (VA41F)
查看詳情 →
POV
2026-04-09
Seaman Pro/Seaman
查看詳情 →
OAS
2026-04-09
RCT800
查看詳情 →
GXN
2026-04-09
EASYMADE-TI
查看詳情 →沒有符合的裝置。
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