FDA Device Intelligence
Home › devemed GmbH › devemed

devemed

devemed GmbH · Model 2302-500 · UDI-DI 04061644023769

EFL Prescription
5
510(k) clearances
2
Adverse events
0
Recalls
201
Facilities

Description

Tissue forceps 1x2 "Semken" 155 mm straight, fine

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.