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FiberLocker Instrument

ZuriMED Technologies AG · Model FL516SNA · UDI-DI 07649988202247

OWX Prescription
2
510(k) clearances
13
Adverse events
0
Recalls
15
Facilities

Description

ZuriMED Technologies AG - FiberLocker Instrument

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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.