FDA Device Intelligence
Home › MEDTRONIC, INC. › ACTtrac®

ACTtrac®

MEDTRONIC, INC. · Model 31363 · UDI-DI 00613994495167

GKN
1
510(k) clearances
335
Adverse events
0
Recalls
3
Facilities

Description

CONSOLE 31363 ACTTRAC HEPARIN MNGMNT 13L

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.