FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model OM236R · UDI-DI 04038653179473

FMA Prescription
5
510(k) clearances
9
Adverse events
0
Recalls
223
Facilities

Description

WEDER Tongue Depressor, 5", (125 mm), small, fenestrated, non-sterile, reusable

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.