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N.A.

Geuder Aktiengesellschaft · Model 33759 · UDI-DI 04049368014157

HNH
7
510(k) clearances
3
Adverse events
0
Recalls
92
Facilities

Description

N.A.

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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.