FDA Device Intelligence
HomeTIDI PRODUCTS, LLC › TIDISHIELD

TIDISHIELD

TIDI PRODUCTS, LLC · Model 20841 · UDI-DI 00618125102419

EGZ
8
510(k) clearances
4
Adverse events
0
Recalls
128
Facilities

Description

X-Ray Sensor Sheaths Fits Cygnus Sensor MPS Size 1 Box of 100

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.