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Active Erection System
KESSEL medintim GmbH · Model AES 01 · UDI-DI 04013273000116
10
510(k) clearances
17
Adverse events
0
Recalls
48
Facilities
Description
Vacuum Erection Device for treatment of erectile dysfunction
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Get your free API keyRead the docsData 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.