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Dornier MedTech

DORNIER MEDTECH AMERICA, INC. · Model SLID3515S · UDI-DI 00810116020676

EYA Prescription
0
510(k) clearances
205
Adverse events
0
Recalls
27
Facilities

Description

Hydrophilic Nitinol Guidewire, 0.035" diameter, 150 cm length, 3 cm tip.

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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.