Home › GCE, s.r.o. › MediMeter
MediMeter
GCE, s.r.o. · Model 0730104US · UDI-DI 08592346749436
10
510(k) clearances
156
Adverse events (15 deaths)
1
Recalls
45
Facilities
Description
Mediflow devices are intended for the administration of the following medical gases in the treatment and care of patients. This flow selector is intended to be fitted to medical gas pipeline system terminal units in hospitals or ambulance cars or to a quick connector outlet of a medical gas regulator.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-08-26 | Porter Instrument Co Inc | inverted check value on the bag tee assembly which can cause leaking of mixed N2O/O2 gas |
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 docsData 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.