FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model OM155R · UDI-DI 04038653207879

FMA Prescription
5
510(k) clearances
9
Adverse events
0
Recalls
222
Facilities

Description

DOUGHTY Tongue Depressor, blade, depth: 76 mm, 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.