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Atmos

DELTA MED SPA · Model UD-A36205 · UDI-DI 08032248487130

EXQ Prescription
8
510(k) clearances
9
Adverse events
1
Recalls
15
Facilities

Description

Pump Tubing 3,2 x 6,4

Recalls

DateFirmReason
2009-04-09Laborie Medical Technologies CorLaborie Medical Technologies reports that there was a mix up in the labeling and packaging of their Urodynamic Catheters. There were 8Fr catheters mixed inside the 6Fr catheter pac

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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.