FDA Device Intelligence
HomeELMED INCORPORATED › ELMED

ELMED

ELMED INCORPORATED · Model 5196 ENT I · UDI-DI 00842180106192

BWA Prescription
3
510(k) clearances
99
Adverse events
0
Recalls
8
Facilities

Description

ESU 70 B ENT I PACKAGE: CONSISTING OF (1) 5196 ESU 70 B GENERATOR, (1) 5701 FOOTSWITCH, (1) 5747 PATIENT PLATE, (1) 5701 PATIENT PLATE RETURN CABLE, (1) 5044 RETAINING STRAP

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.