FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model DL242R · UDI-DI 04038653148134

EMJ Prescription
6
510(k) clearances
641
Adverse events
0
Recalls
237
Facilities

Description

HEIDBRINK Root Apex Elevator, angled, delicate, double ended, round handle, Fig. 2, 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.