FDA Device Intelligence
HomeGimmi GmbH › Gimmi

Gimmi

Gimmi GmbH · Model UV.1604.10 · UDI-DI 04049047779346

HHM Prescription
10
510(k) clearances
92
Adverse events
4
Recalls
132
Facilities

Description

GUYON DILATING BOUGIE CURVED, WITHOUT INTERNAL THREAD, 10 CH. LENGTH 270 MM

Recalls

DateFirmReason
2024-07-31CooperSurgical, Inc.During the manufacturing process the devices were laser-marked with the incorrect part number.
2024-07-31CooperSurgical, Inc.During the manufacturing process the devices were laser-marked with the incorrect part number.
2019-12-11Centurion Medical Products CorporationIncomplete seals on the sterile package may compromise the sterility
2016-10-28Hologic, IncBreach in sterile barrier compromising product sterility

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.