FDA Device Intelligence
Home › MEDLINE INDUSTRIES, INC. › Medline

Medline

MEDLINE INDUSTRIES, INC. · Model DYND17407 · UDI-DI 10884389119495

FFG Prescription
10
510(k) clearances
563
Adverse events
1
Recalls
37
Facilities

Description

METER,URINE,EXACT MEASURE,200ML,LF,LL

Recalls

DateFirmReason
2023-12-04Cardinal Health 200, LLCConvenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

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.