FDA Device Intelligence
Home › Wenzhou Caretek Medical Device Co., Ltd. › DIXIEEMS

DIXIEEMS

Wenzhou Caretek Medical Device Co., Ltd. · Model 422602R · UDI-DI 06975871430260

LDE
10
510(k) clearances
29
Adverse events
0
Recalls
179
Facilities

Description

RED SPRAGUE STETHOSCOPE

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.