MXK
2026-03-13
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
MTD
2026-03-13
OptiMap Catheter - 50mm (OPTI-CATH2-50)
查看詳情 →
LPL
2026-03-13
Pegavision (Toufilcon B) Daily Disposable Soft (Hydrophilic) Contact Lenses; Pegavision (Toufilcon B) Soft (Hydrophilic) Contact Lenses
查看詳情 →
QIH
2026-03-13
InferCare RECIST
查看詳情 →
DXF
2026-03-13
SafeSept RF Transseptal Guidewire (SSRF132; SSRF132R; SSRF232; SSRF232R; SSRF135; SSRF135R; SSRF235; SSRF235R)
查看詳情 →
GWQ
2026-03-13
New Wave System
查看詳情 →
SEI
2026-03-13
Access anti-HBc IgM
查看詳情 →
LNH
2026-03-13
Embrace Neonatal MRI System
查看詳情 →
FGE
2026-03-13
BARE Wireguided Balloon Dilation Catheter (1235)
查看詳情 →
GXP
2026-03-13
Permatage Flowable, Settable Bone Paste
查看詳情 →
JKA
2026-03-13
BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes
查看詳情 →
PCU
2026-03-13
Niti-S SPAXUS Stent
查看詳情 →沒有符合的裝置。
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