FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model OG073R · UDI-DI 04046964073229

KAT Prescription
0
510(k) clearances
38
Adverse events
0
Recalls
19
Facilities

Description

Micro Ear Needle, straight, 6 1/4", (160 mm), diam. 0,60 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.