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Quinelato

Schobell Industrial Ltda · Model QD.676.02 · UDI-DI 07898506854134

EMK Prescription
1
510(k) clearances
1
Adverse events
0
Recalls
130
Facilities

Description

Tunneling instrument angled

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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.