FDA Device Intelligence
HomeNATEC MEDICAL LTD › FILAO NC PTCA Dilatation Catheter

FILAO NC PTCA Dilatation Catheter

NATEC MEDICAL LTD · Model N023_25-25US · UDI-DI 06091403537709

LOX Prescription
10
510(k) clearances
43,512
Adverse events (583 deaths)
121
Recalls
77
Facilities

Description

FILAO NC PTCA Dilatation Catheter, 3.25 X 25 MM/ Shaft length 140 CM

Recalls

DateFirmReason
2022-06-24Medtronic IncLuer has balloon diameter printed as "2.25mmx12mm" instead of the correct diameter, "2.5mmx12mm" as reflected on the product outer packaging.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29Abbott VascularCoronary Dilatation Catheters may exhibit difficulty or inability to deflate 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.