FDA Device Intelligence
HomeLepu Medical Technology (Beijing) Co.,Ltd. › Angioway

Angioway

Lepu Medical Technology (Beijing) Co.,Ltd. · Model LP-P-30-YNP · UDI-DI 06936733735930

PTLDTLPTM Prescription
0
510(k) clearances
0
Adverse events
0
Recalls
33
Facilities

Description

Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.