FDA Device Intelligence
HomeAMD Medicom Inc › AMD-RITMED

AMD-RITMED

AMD Medicom Inc · Model 53803 · UDI-DI 20686864042963

EYZ
10
510(k) clearances
44
Adverse events
1
Recalls
50
Facilities

Description

AMD-RITMED GT DRAINAGE BAGS WITH SPOUT

Recalls

DateFirmReason
2017-03-09C.R. Bard, Inc.Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex.

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.