Mindray DS USA, Inc.
Mindray DS USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2013, with 8 FDA device recalls on record.
Top product codes for Mindray DS USA, Inc.
FDA recalls by Mindray DS USA, Inc.
- Z-0109-2027 — ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM 15M/ePM 10A
- Z-0110-2027 — BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.
- Z-0112-2027 — Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).
- Z-0111-2027 — BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80
- Z-0115-2027 — cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
- Z-0113-2027 — BeneView Series. Operator's Manuals: T5 / T8
- Z-0116-2027 — T1 Patient Monitor. Operator's Manual: T1 Patient Monitor
- Z-0114-2027 — Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V
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 Mindray DS USA, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.