FDA Device Intelligence
Home › Gimmi GmbH › Gimmi

Gimmi

Gimmi GmbH · Model AD.1059.14 · UDI-DI 04049047014348

KCH Prescription
0
510(k) clearances
5
Adverse events
0
Recalls
79
Facilities

Description

JACKSON TRAQUEA RETRACTOR DOUBLE-ENDED LENGTH 150 MM

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.