FDA Device Intelligence
Home › Covidien LP › BIS

BIS

Covidien LP · Model 186-0108-RFB · UDI-DI 10884521175501

OLW Prescription
1
510(k) clearances
347
Adverse events (1 deaths)
1
Recalls
35
Facilities

Description

OEM A2000 Simulator Demo,Refurbished

Recalls

DateFirmReason
2018-07-26Covidien LLCRevised replacement instructions for the Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems

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.