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HeliO2 Blender

Precision Medical, Inc. · Model PM5470 · UDI-DI 00855887006047

BZR Prescription
1
510(k) clearances
590
Adverse events (9 deaths)
3
Recalls
40
Facilities

Description

PM5400 SERIES,BLENDER,HE/O2,LOW FLOW,70/30

Recalls

DateFirmReason
2018-05-15CAREstream Medical LLCTwo analgesic gas delivery system oxygen/nitrous oxide mixers were reported to have delivered higher levels of nitrous oxide than specification during routine testing.
2018-05-14O-Two Medical Technologies, Inc.Higher levels of nitrous oxide delivered than specification
2005-01-11Maquet IncSoftware update so US customers will be updated equally with worldwide customers. Ver. 5.0 will be upgraded to ver 7.0. Quality will improve and enhance functionality.

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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.