Home › WELCH ALLYN, INC. › Welch Allyn, Inc.
Welch Allyn, Inc.
WELCH ALLYN, INC. · Model 901006 · UDI-DI 00732094281682
1
510(k) clearances
33
Adverse events (4 deaths)
2
Recalls
48
Facilities
Description
Blue Max electrodes, wet gel, foam, offset snap, round 46mm (1.81 in.), 25 electrodes/pouch. 40pouches per case. Price per case.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate |
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate |
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.
