AIM PLUS AMBULATORY INFUSION PUMP
by Unknown
The AIM PLUS AMBULATORY INFUSION PUMP by Unknown has a safety score of 82 out of 100, placing it in the low-risk category. Based on FDA MAUDE data, there have been 40 adverse event reports since its introduction in 2015. With an estimated 0 units in use, the incident rate is 0 per 10,000 units. It ranks #8 out of 234 devices in the Infusion Pumps category.
Adverse Events
Total reports filed with FDA MAUDE
Death Reports
Death reports associated with device
Incident Rate
Per 10,000 units in use
Recalls
No recalls on record
Estimated Units in Use
Based on market data estimates
Category Ranking
In Infusion Pumps by safety score
How This Compares
Other Infusion Pumps Devices
SERIES 3001 INTRA-AORTIC BALLOON PUMP
Unknown
SIGNATURE EDITION INFUSION PUMP
Unknown
PUMP MMT-512LNAL PRDGM INS CL EN US LN
Unknown
ART PILLOW 8MM PUMP SEGM UNIVE
Unknown
Important Context
Adverse event reports reflect reported incidents, not confirmed device failures. Higher numbers may indicate greater device usage, better reporting systems, or increased awareness. This data should be one factor in your research — always consult your physician.