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Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH · Model H118-12014 · UDI-DI 04059453047342

EIG
8
510(k) clearances
34
Adverse events
0
Recalls
337
Facilities

Description

ROUX retractor double, fig.1, 5 1/2", 14cm

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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.