FDA Device Intelligence
HomeGuangzhou Decheng Biotechnology Co., LTD › UScreen

UScreen

Guangzhou Decheng Biotechnology Co., LTD · Model USSCUPA-10MOB-300 · UDI-DI 00850065976136

NGLNFTPTHNFVNFYPTGNGGNGMQBFQAWDJGNFW
1
510(k) clearances
1
Adverse events
0
Recalls
58
Facilities

Description

UScreen™ RAPID DRUG TEST CUP, 10-Panel, 25T/Box

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.