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PIRAEUS MEDICAL INC.

2 clearances · 2 inspections · aggregated across 2 source records

Scorecard
Events per device across the 11-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.

MAUDE reports per device

0

0 in the last 12 months

Higher volume than 83% of companies with 10+ devices

Recalls per device

0

0 in the last 12 months

Higher volume than 97% of companies with 10+ devices

These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.

Devices
11 device records · ordered by linked event volume.
BrandModelProduct codesPrimary DILinked events
87 NeuGlide Catheter103577-002DQY QJP008600103063141
87 NeuGlide Catheter103577-001DQY QJP008600103063071
87 NeuGlide Catheter103577-006DQY QJP008600155277691
87 NeuGlide Catheter103577-005DQY QJP008600155277521
87 NeuGlide Catheter103577-004DQY QJP008600103063211
87 NeuGlide+ Catheter100650-004DQY QJP008600155277071
87 NeuGlide+ Catheter100650-003DQY QJP008600103063761
87 NeuGlide+ Catheter100650-002DQY QJP008600103063691
87 NeuGlide+ Catheter100650-005DQY QJP008600155277141
93 NeuFlex Catheter100148-002DQY QJP008600103063451
93 NeuFlex Catheter100148-001DQY QJP008600103063381
Facilities
Registered establishments with their latest FDA inspection outcome.
FEINameLocationLast inspectionWatch
3031768596PIRAEUS MEDICAL, INC.Maple Grove, MN, USNAI