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TubaVent® balloon dilatation system

Spiggle & Theis Medizintechnik GmbH · Model 2080-3045-US · UDI-DI 04250676745088

PNZ Prescription
1
510(k) clearances
31
Adverse events
0
Recalls
16
Facilities

Description

TubaInsert ONE® - Type 45°, insertion device, sterile, 10 pieces

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

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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.