FDA Device Intelligence
Homemahe medical gmbh › mahe medical GmbH

mahe medical GmbH

mahe medical gmbh · Model 35.005.02 · UDI-DI 04050659367869

FDC
10
510(k) clearances
442
Adverse events (2 deaths)
0
Recalls
37
Facilities

Description

Telescope bridge w.2 working channels, _x000D_for 4.0mm optic _x000D_

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.