Mediana Co., Ltd.
Mediana Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Mediana Co., Ltd.
FDA recalls by Mediana Co., Ltd.
- Z-2096-2021 — AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and hospital-type facilities.
- Z-2441-2020 — DIRECT SUPPLY Attendant VITAL SIGNS MONITOR, REF AVSM2 - Product Usage: It is vital sign monitor to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and hospital-type facilities.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Mediana Co., Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.