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NA

aap Implantate AG · Model IU 7840-00 · UDI-DI 04042409041891

HXX Prescription
4
510(k) clearances
23,401
Adverse events (4 deaths)
0
Recalls
465
Facilities

Description

Screwdriver, hexagonal ø2.5

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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.